Methods for making composite products containing lignocellulose substrates

ABSTRACT

A method for making a composite product can include combining a plurality of lignocellulose substrates and a binder to produce a resinated furnish. The binder can be or include a polyphenolic compound, a free radical precursor, and an unsaturated compound having two or more unsaturated carbon-carbon bonds. At least one of the unsaturated carbon-carbon bonds is a pi-bond that is not conjugated with an aromatic moiety and is capable of free radical addition. The method can also include pressing the resinated furnish between at least two surfaces in a press, where at least one of the at least two surfaces can be a porous surface, and at least partially curing the binder in the resinated furnish to produce a composite product.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation-in-part of U.S. patent application Ser. No. 14/205,431 (now U.S. Pat. No. 9,243,114), filed Mar. 12, 2014, which claims benefit to U.S. Provisional Patent Application No. 61/782,302, filed Mar. 14, 2013, which are both incorporated by reference herein.

BACKGROUND

Field

Embodiments described generally relate to binder compositions that include one or more polyphenolic compounds, one or more unsaturated compounds, and one or more free radical precursors and methods for making and using same.

Description of the Related Art

The production of lignocellulose composite products requires an adhesive or binder to bond the discrete, particulates, fibers, veneers, or other substrates to one another. Typical lignocellulose composite products include particleboard, fiberboard, oriented strand board (OSB), or plywood. Conventional binders used in the production of these products frequently contain formaldehyde based resins, such as urea-formaldehyde (UF), melamine-formaldehyde (MF), melamine-urea-formaldehyde (MUF), and phenol-formaldehyde (PF). While these formaldehyde based resins produce finished products having desirable properties, such as strength, these formaldehyde based resins also release formaldehyde into the environment during the production of the binder and the curing of the binder in the manufacture of a lignocellulose composite product, as well as, from the final composite product made using the binder.

Various techniques have been used to reduce the amount of formaldehyde released from formaldehyde based resins. For example, the addition of formaldehyde scavengers to the resin and/or various modifications to the particular synthesis steps used to make the formaldehyde based resin, such as the addition of urea as a reactant late in the binder synthesis, are often used in an attempt to reduce formaldehyde emission. These attempts to reduce formaldehyde emission, however, are accompanied with undesirable effects such as longer cure time, reduced resin shelf-life, reduced product strength, reduced tolerance for processing variations, and/or inferior moisture resistance.

There is a need, therefore, for improved methods for making composite products having reduced or no formaldehyde emission.

SUMMARY

Methods for making composite products are provided. In one or more embodiments, a method for making a composite product can include combining a plurality of lignocellulose substrates and a binder to produce a resinated furnish. The binder can be or include a polyphenolic compound, a free radical precursor, and an unsaturated compound having two or more unsaturated carbon-carbon bonds. At least one of the unsaturated carbon-carbon bonds is a pi-bond (π-bond) that is not conjugated with an aromatic moiety and is capable of free radical addition. The method can also include pressing the resinated furnish between at least two surfaces in a press and at least partially curing the binder in the resinated furnish to produce a composite product. At least one of the at least two surfaces can be a porous surface.

In some embodiments, the method for making a composite product can include combining the plurality of lignocellulose substrates and the binder to produce the resinated furnish and heating at least two surfaces in a press to a temperature of 110° C. to about 180° C. At least one of the at least two surfaces in the press can be a porous surface. The method can also include heating and pressing the resinated furnish between the at least two surfaces and at least partially curing the binder in the resinated furnish to produce a composite product. A core of the composite product can be heated by the at least two surfaces to a maximum internal board temperature of about 100° C. to about 165° C.

In other embodiments, the method for making the composite product can include that the binder can be or include the polyphenolic compound, the free radical precursor, and the unsaturated compound that can include an unsaturated polyester prepolymer, an unsaturated polyether prepolymer, an unsaturated polyamide prepolymer, an unsaturated polyurethane prepolymer, or any mixture thereof. The method also includes heating and pressing the resinated furnish between at least two surfaces in a press and at least partially curing the binder in the resinated furnish to produce the composite product. At least one of the at least two surfaces can be a porous surface that can be or include a press screen, a caul screen, a caul plate, a mesh screen, a press weave, or a perforated platen.

In other embodiments, binder compositions and methods for making and using same are provided. In some embodiments, the binder composition can include at least one polyphenolic compound, at least one unsaturated compound, and at least one free radical precursor. The unsaturated compound can have two or more unsaturated carbon-carbon bonds. At least one of the unsaturated carbon-carbon bonds can be a pi-bond that is not conjugated with an aromatic moiety and is capable of free radical addition.

In other embodiments, the binder composition can include at least one polyphenolic compound, at least one unsaturated compound, at least one oxidant, and at least one catalyst. The unsaturated compound can have two or more unsaturated carbon-carbon bonds. At least one of the unsaturated carbon-carbon bonds can be a pi-bond that is not conjugated with an aromatic moiety and is capable of free radical addition.

In some embodiments, the method for making a composite product can include combining a plurality of lignocellulose substrates, at least one polyphenolic compound, at least one unsaturated compound, and at least one free radical precursor to produce a mixture. The unsaturated compound can have two or more unsaturated carbon-carbon bonds. At least one of the unsaturated carbon-carbon bonds can be a pi-bond that is not conjugated with an aromatic moiety and is capable of free radical addition. The method can also include heating the mixture to a temperature of about 60° C. to about 300° C. to produce a composite product.

In other embodiments, the method for making a composite product can include combining a plurality of lignocellulose substrates with a binder composition. The binder composition can include at least one polyphenolic compound, at least one unsaturated compound, at least one oxidant, and at least one catalyst. The unsaturated compound can have two or more unsaturated carbon-carbon bonds. At least one of the unsaturated carbon-carbon bonds can be a pi-bond that is not conjugated with an aromatic moiety and is capable of free radical addition.

In some embodiments, the composite product can include a plurality of lignocellulose substrates and an at least partially cured binder composition. Prior to at least partial curing, the binder composition can include at least one polyphenolic compound, at least one unsaturated compound, and at least one free radical precursor. The unsaturated compound can have two or more unsaturated carbon-carbon bonds. At least one of the unsaturated carbon-carbon bonds can be a pi-bond that is not conjugated with an aromatic moiety and is capable of free radical addition.

In other embodiments, the composite product can include a plurality of lignocellulose substrates and an at least partially cured binder composition. Prior to at least partial curing, the binder composition can include at least one polyphenolic compound, at least one unsaturated compound, at least one oxidant, and at least one catalyst. The unsaturated compound can have two or more unsaturated carbon-carbon bonds. At least one of the unsaturated carbon-carbon bonds can be a pi-bond that is not conjugated with an aromatic moiety and is capable of free radical addition.

DETAILED DESCRIPTION

In one or more embodiments, a plurality of lignocellulose substrates and one or more binders can be mixed, blended, stirred, contacted, or otherwise combined with one another to produce a mixture. The mixture can also be referred to as a “furnish,” “blended furnish,” “resinated mixture,” “resinated furnish,” or “mat.” The binder can be or include one or more polyphenolic compounds, one or more free radical precursors, and one or more unsaturated compounds having two or more unsaturated carbon-carbon bonds. At least one of the unsaturated carbon-carbon bonds can be a pi-bond that is not conjugated with an aromatic moiety and is capable of free radical addition. The resinated furnish can be pressed between at least two surfaces in a press. At least one of the at least two surfaces can be a porous surface. The binder in the resinated furnish can be at least partially cured to produce a composite product.

As used herein, the terms “unsaturated compound” and “reactive unsaturated compound” are used interchangeably and refer to compounds having two or more unsaturated carbon-carbon bonds, where at least one of the unsaturated carbon-carbon bonds is capable of free radical addition. As used herein, the phrase “capable of free radical addition” when used in conjunction with “unsaturated compound” means that the carbon-carbon double bond is a pi-bond (π-bond) that is not conjugated with an aromatic moiety and is capable of going through a free radical chain reaction mechanism. The free radical chain mechanism can include an initiation step, a propagation step, and a termination step. In one or more embodiments, the unsaturated carbon-carbon bond capable of free radical addition can be of an alkene conjugated with a carbonyl group in an α,β-unsaturated carbonyl compound. The α,β-unsaturated carbonyl compound can include, but is not limited to, an aldehyde, a ketone, a carboxylic acid, an ester, an amide, an acyl halide, an acid anhydride, or an imide. For example, the α,β-unsaturated carbonyl compound can be, but is not limited to, an α,β-unsaturated aldehyde (e.g., an enal), an α,β-unsaturated ketone (e.g., an enone), an α,β-unsaturated carboxylic acid, an α,β-unsaturated ester, an α,β-unsaturated amide, an α,β-unsaturated acyl halide, an α,β-unsaturated acid anhydride, or an α,β-unsaturated imide. In one or more embodiments, the unsaturated compound can be substantially free or completely free from any aromatic moiety.

The polyphenolic compound can be present in the binder composition in an amount of about 1 wt %, about 5 wt %, about 10 wt %, about 15 wt %, about 20 wt %, about 25 wt %, about 30 wt %, or about 35 wt % to about 55 wt %, about 60 wt %, about 65 wt %, about 70 wt %, about 75 wt %, about 80 wt %, about 85 wt %, about 90 wt %, about 95 wt %, or about 99 wt %, based on the combined weight of the polyphenolic compound, the unsaturated compound, and the free radical precursor. For example, the polyphenolic compound can be present in the binder composition in an amount of about 20 wt % to about 60 wt %, about 30 wt % to about 60 wt %, about 35 wt % to about 55 wt %, about 40 wt % to about 50 wt %, about 45 wt % to about 65 wt %, about 50 wt % to about 75 wt %, or about 55 wt % to about 85 wt %, based on the combined weight of the polyphenolic compound, the unsaturated compound, and the free radical precursor.

The polyphenolic compound can be present in the binder composition in an amount of about 1 wt %, about 5 wt %, about 10 wt %, about 15 wt %, about 20 wt %, about 25 wt %, about 30 wt %, or about 35 wt % to about 55 wt %, about 60 wt %, about 65 wt %, about 70 wt %, about 75 wt %, about 80 wt %, about 85 wt %, about 90 wt %, about 95 wt %, or about 99 wt %, based on the combined weight of the polyphenolic compound and the unsaturated compound. For example, the polyphenolic compound can be present in the binder composition in an amount of about 20 wt % to about 60 wt %, about 30 wt % to about 60 wt %, about 35 wt % to about 55 wt %, about 40 wt % to about 50 wt %, about 45 wt % to about 65 wt %, about 50 wt % to about 75 wt %, about 50 wt % to about 70 wt %, about 55 wt % to about 65 wt %, or about 55 wt % to about 85 wt %, based on the combined weight of the polyphenolic compound and the unsaturated compound.

The unsaturated compound can be present in the binder composition in an amount of about 5 wt %, about 10 wt %, about 15 wt %, about 20 wt %, or about 25 wt % to about 40 wt %, about 45 wt %, about 50 wt %, about 55 wt %, about 60 wt %, about 65 wt %, or about 70 wt %, based on the combined weight of the polyphenolic compound, the unsaturated compound, and the free radical precursor. For example, the unsaturated compound can be present in the binder composition in an amount of about 15 wt % to about 45 wt %, about 20 wt % to about 40 wt %, 25 wt % to about 35 wt %, about 30 wt % to about 40 wt %, about 40 wt % to about 55 wt %, or about 30 wt % to about 60 wt %, based on the combined weight of the polyphenolic compound, the unsaturated compound, and the free radical precursor.

The unsaturated compound can be present in the binder composition in an amount of about 5 wt %, about 10 wt %, about 15 wt %, about 20 wt %, or about 25 wt % to about 40 wt %, about 45 wt %, about 50 wt %, about 55 wt %, about 60 wt %, about 65 wt %, about 70 wt %, or about 75 wt %, based on the combined weight of the polyphenolic compound and the unsaturated compound. For example, the unsaturated compound can be present in the binder composition in an amount of about 15 wt % to about 45 wt %, about 20 wt % to about 40 wt %, 25 wt % to about 35 wt %, about 35 wt % to about 45 wt %, about 30 wt % to about 40 wt %, about 40 wt % to about 55 wt %, or about 30 wt % to about 60 wt %, based on the combined weight of the polyphenolic compound and the unsaturated compound.

The free radical precursor can be present in the binder composition in an amount of about 5 wt %, about 10 wt %, about 20 wt %, about 30 wt %, about 40 wt %, about 50 wt %, about 60 wt %, about 70 wt %, or about 80 wt % to about 120 wt %, about 130 wt %, about 140 wt %, about 150 wt %, about 160 wt %, about 170 wt %, about 180 wt %, about 190 wt %, or about 200 wt %, based on the weight of the polyphenolic compound. For example, the free radical precursor can be present in the binder composition in an amount of about 25 wt % to about 95 wt %, about 35 wt % to about 85 wt %, about 45 wt % to about 85 wt %, about 45 wt % to about 65 wt %, about 50 wt % to about 60 wt %, about 55 wt % to about 75 wt %, or about 45 wt % to about 60 wt %, based on the weight of the polyphenolic compound.

The free radical precursor can be present in the binder composition in an amount of about 10 wt %, about 30 wt %, about 50 wt %, about 70 wt %, about 90 wt %, about 110 wt %, or about 130 wt % to 160 wt %, about 180 wt %, about 200 wt %, about 220 wt %, about 240 wt %, about 260 wt %, about 280 wt %, or about 300 wt %, based on the weight of the unsaturated compound. For example, the free radical precursor can be present in the binder composition in an amount of about 30 wt % to about 100 wt %, about 40 wt % to about 95 wt %, about 65 wt % to about 105 wt %, about 70 wt % to about 90 wt %, about 75 wt % to about 85 wt %, about 75 wt % to about 80 wt %, about 80 wt % to about 95 wt %, about 80 wt % to about 155 wt %, about 70 wt % to about 150 wt %, or about 60 wt % to about 145 wt %, based on the weight of the unsaturated compound.

The free radical precursor can be present in the binder composition in an amount of about 5 wt %, about 8 wt %, about 12 wt %, about 14 wt %, about 18 wt %, about 22 wt %, about 26 wt %, or about 28 wt % to about 40 wt %, about 45 wt %, about 50 wt %, about 55 wt %, about 60 wt %, about 65 wt %, or about 70 wt %, based on the combined weight of the polyphenolic compound, the unsaturated compound, and the free radical precursor. For example, the free radical precursor can be present in the binder composition in an amount of about 5 wt % to about 45 wt %, about 15 wt % to about 25 wt %, about 10 wt % to about 20 wt %, about 20 wt % to about 30 wt %, about 25 wt % to about 40 wt %, about 25 wt % to about 50 wt %, about 30 wt % to about 60 wt %, about 40 wt % to about 70 wt %, or about 15 wt % to about 55 wt %, based on the combined weight of the polyphenolic compound, the unsaturated compound, and the free radical precursor.

The binder composition can have a viscosity of about 1 cP, about 20 cP, about 100 cP, 1,000 cP, about 5,000 cP, or about 10,000 cP to about 50,000 cP, about 100,000 cP, about 200,000 cP, or about 300,000 cP at a temperature of 25° C. For example, the binder composition can have a viscosity of about 20 cP to about 50,000 cP, about 500 cP to about 25,000 cP, about 15,000 cP to about 45,000 cP, or about 3,000 cP to about 40,000 cP at a temperature of about 25° C. The viscosity of the binder composition and/or any other composition discussed and described herein can be determined using a viscometer at a temperature of about 25° C. For example, a Brookfield Viscometer, Model DV-II+, with a small sample adapter with, for example, a number 3 spindle, can be used. The small sample adapter can allow the sample to be cooled or heated by the chamber jacket to maintain the temperature of the sample surrounding the spindle at a temperature of about 25° C.

The pH of the binder composition can be acidic, neutral, or basic. For example, the pH of the binder composition can be about 0.5, about 2, about 3, or about 4 to about 7, about 7.5, about 8, about 8.5, or about 9. For example, the binder composition can have a pH of about 1.5 to about 9, about 2.5 to about 7, about 1 to about 5, about 5 to about 8, or about 3 to about 6. The pH of the binder composition can be adjusted to any desired pH by combining one or more base compounds, one or more acid compounds, or a combination of one or more base compounds and one or more acid compounds therewith.

Illustrative base compounds that can be used to adjust the pH of the binder composition can include, but are not limited to, hydroxides, carbonates, ammonia, amines, any combination thereof. Illustrative hydroxides can include, but are not limited to, sodium hydroxide, potassium hydroxide, ammonium hydroxide (e.g., aqueous ammonia), lithium hydroxide, and cesium hydroxide. Illustrative carbonates can include, but are not limited to, sodium carbonate, sodium bicarbonate, potassium carbonate, and ammonium carbonate. Illustrative amines can include, but are not limited to, trimethylamine, triethylamine, triethanolamine, diisopropylethylamine (Hunig's base), pyridine, 4-dimethylaminopyridine (DMAP), and 1,4-diazabicyclo[2.2.2]octane (DABCO).

Illustrative acid compounds that can be used to adjust the pH of the binder composition can include, but are not limited to, one or more mineral acids, one or more organic acids, one or more acid salts, or any combination thereof. Illustrative mineral acids can include, but are not limited to, hydrochloric acid, nitric acid, phosphoric acid, sulfuric acid, or any combination thereof. Illustrative organic acids can include, but are not limited to, acetic acid, formic acid, citric acid, oxalic acid, uric acid, lactic acid, or any combination thereof. Illustrative acid salts can include, but are not limited to, ammonium sulfate, sodium, sodium bisulfate, sodium metabisulfite, or any combination thereof.

The polyphenolic compound can be or include, but is not limited to, one or more lignins, one or more tannins, one or more novolac resins, one or more modified phenol formaldehyde resins, bisphenol A, humic acid, modified polyphenolic compounds, or any combination or mixture thereof.

The polyphenolic compound can be in the form of a solid, a solution, or a solid/liquid “two phase” mixture, such as a slurry, an emulsion, a suspension, or a dispersion. The solution or other solid/liquid mixture can include one or more liquid mediums. The liquid medium can be or include, but is not limited to, water, alcohols, glycols, glycol ethers, acetonitrile, dimethyl sulfoxide, N,N-dimethylformamide, N-methylpyrrolidone, any combination thereof, or any mixture thereof. Suitable alcohols can include, but are not limited to, methanol, ethanol, propanol, isopropanol, butanol, isomers thereof, any combination thereof, or any mixture thereof. Suitable glycols can include, but are not limited to, ethylene glycol, propylene glycol, or a combination thereof. As used herein, the terms “aqueous medium” and “aqueous liquid” are used interchangeably and can be or include water and/or mixtures composed of water and/or other water-miscible solvents. Illustrative water-miscible solvents can include, but are not limited to, alcohols, ethers, amines, other polar aprotic solvents, and the like.

The solution or solid/liquid mixture of the polyphenolic compound and the liquid medium can include about 0.1 wt %, about 5 wt %, about 10 wt %, about 20 wt %, about 30 wt %, or about 40 wt % to a high of about 70 wt %, about 80 wt %, about 90 wt %, about 95 wt % about 99 wt %, or about 99.9 wt % of the polyphenolic compound, based on the combined weight of the polyphenolic compound and the liquid medium. For example, the solution or solid/liquid mixture can include about 0.1 wt % to about 30 wt %, about 1 wt % to about 20 wt %, about 5 wt % to about 50 wt %, about 10 wt % to about 70 wt %, about 0.5 wt % to about 25 wt %, about 3 wt % to about 6 wt %, or about 2 wt % to about 8 wt % of the polyphenolic compound, based combined weight of the polyphenolic compound and the liquid medium. In another example, the solution or solid/liquid mixture can include about 0.1 wt % to about 10 wt %, about 1 wt % to about 12 wt %, about 2 wt % to about 9 wt %, about 3 wt % to about 9 wt %, about 5 wt % to about 15 wt %, about 4 wt % to about 6 wt %, about 8 wt % to about 20 wt %, or about 2 wt % to about 10 wt % of the polyphenolic compound, based combined weight of the polyphenolic compound and the liquid medium.

As used herein, the solids concentration or solids content of the solution or solid/liquid mixture of the polyphenolic compound and the liquid medium, as understood by those skilled in the art, can be measured by determining the weight loss upon heating a small sample, e.g., 1-5 grams of the solution or solid/liquid mixture of the polyphenolic compound and the liquid medium, to a suitable temperature, e.g., 125° C., and a time sufficient to remove any liquid combined therewith. By measuring the weight of the sample before and after heating, the percent solids in the sample can be directly calculated or otherwise estimated.

Suitable solid polyphenolic compounds can be in the form of a powder, flakes, or other solid form. If the polyphenolic compound is in the form of a powder, the polyphenolic compound can have an average particle size of about 0.05 microns, about 0.1 micron, about 0.6 microns, about 1 micron, about 5 microns, about 7 microns or about 10 microns to about 115 microns, about 225 microns, about 350 microns, about 425 microns, or about 500 microns. In another example, the polyphenolic compound can have an average particle size of about 0.3 microns to about 160 microns, about 22 microns to about 48 microns, about 35 microns to about 60 microns, about 50 microns to about 75 microns or about 70 microns to about 120 microns about 30 microns to about 70 microns, about 60 microns to about 150 microns, about 100 microns to about 200 microns, about 175 microns to about 325 microns, about 220 microns to about 400 microns, or about 385 microns to about 500 microns.

Lignin is a polymeric substance that can include substituted aromatics found in plant and vegetable matter associated with cellulose and other plant constituents. Illustrative plant and vegetable matter can include, but is not limited to, straw, hemp, sisal, cotton stalk, wheat, bamboo, sabai grass, rice straw, banana leaves, paper mulberry (e.g., bast fiber), abaca leaves, pineapple leaves, esparto grass leaves, fibers from the genus Hesperaloe in the family Agavaceae jute, salt water reeds, palm fronds, flax, ground nut shells, hardwoods, softwoods, recycled fiberboards such as high density fiberboard, medium density fiberboard, low density fiberboard, oriented strand board, particleboard, or any combination thereof. For example, the plant matter can be or include wood, for example hardwoods, softwoods, or a combination thereof. Illustrative types of wood can include, but are not limited to, alder, ash, aspen, basswood, beech, birch, cedar, cherry, cottonwood, cypress, elm, fir, gum, hackberry, hickory, maple, oak, pecan, pine, poplar, redwood, sassafras, spruce, sycamore, walnut, and willow.

The lignin can be extracted, separated, or otherwise recovered from the wood, plant, and/or vegetable matter using any of a number of established processes. For example, in the pulp and paper industry, lignin-containing materials such as wood, straw, corn stalks, bagasse, and other vegetable and plant tissues can be processed to recover the cellulose or pulp via a known kraft or sulfate process or a known sulfite process. The residual pulping liquors that include the lignin as a by-product can be a source of lignin. The chemical structure of lignin can vary and the variation can depend, at least in part, on the particular plant from which the lignin is recovered from, location the plant was grown, and/or on the particular method used in recovery or isolation of the lignin from the plant and/or vegetable matter. Lignin can include active groups, such as active hydrogens and/or phenolic hydroxyl groups through which crosslinking or bridging can be effected.

One process for recovering lignin can be or include the process commonly referred to as the organosolve process. The organosolve process uses an organic solvent to solubilize lignin and hemicelluloses. The organosolve process can include contacting lignocellulose material, e.g., wood chips or particles, with an aqueous organic solvent at a temperature of about 130° C., about 140° C., or about 150° C. to about 200° C., about 220° C., or about 230° C. The lignin can break down by hydrolytic cleavage of alpha aryl-ether links into fragments that can be solubilized in the solvent system. Illustrative solvents can include, but are not limited to, acetone, methanol, ethanol, butanol, ethylene glycol, formic acid, acetic acid, or any mixture thereof. The aqueous organic solvent can have a concentration of the solvent in water of about 30 wt %, about 40 wt % or about 50 wt % to about 70 wt %, about 80 wt %, or about 90 wt %.

Since the lignin separated from the plant can be chemically altered from that found in the plant, the term “lignin,” can also refer to lignin products obtained upon separation from the cellulose or recovered from the plant matter. For example, in a sulfite pulping process, the lignocellulose material can be digested with a bisulfite or sulfite resulting in the at least partial sulfonation of the lignin. As such, the lignin can optionally be subjected to further cleavage and/or other modifications such as alkaline treatment or reaction with other constituents to decrease the sulfonate or sulfur content and/or increase the active groups. For example, the lignin can be include about 1.5 wt % to about 5 wt % of a phenolic hydroxyl content and less than 3 wt % of a sulfonate or sulfur content. In other methods of recovery or separation of lignin from wood, plant, or vegetable material, the lignin may not be sulfonated, but could be chemically altered somewhat in some other manner. For example, in residual pulping liquors obtained in sulfate or other alkaline pulping processes, the lignin can be present as an alkali metal salt dissolved in the alkaline, aqueous liquor and can generally include a sufficient phenolic hydroxyl content to require no further modification. However, the alkali or kraft lignin can be further reacted with other constituents to further increase the active groups. “Hydrolysis lignin” that can be recovered from the hydrolysis of lignocellulose materials in the manufacture of sugar, for example, can also be altered somewhat from that found in the plant. As such hydrolysis lignin can be further modified to solubilize the lignin as well as to increase the phenolic hydroxyl content. Also, the lignin products such as residual pulping liquor may be subjected to various treatments such as, for example, acid, alkaline or heat treatments or reacted with the other chemicals which may further alter somewhat the lignin constituents.

The residual pulping liquors or the lignin products produced in the separation or recovery of lignin from the plant matter can include lignin of various weight average molecular weights (MW) of about 300 to about 100,000 or greater. For example, the lignin can have a MW of about 500, about 1,000, about 5,000, about 10,000, about 15,000, or about 20,000 to about 30,000, about 45,000, about 55,000, about 70,000, about 80,000, about 85,000, about 90,000, or about 95,000. In another example, the lignin can have a MW of about 300, about 500, about 800, about 900, about 1,000, or about 1,100 to about 1,300, about 1,500, about 1,900, about 2,300, about 2,500, about 2,700, about 3,000, about 3,300, about 3,500, about 3,700, about 4,000, about 4,300, about 4,500, about 4,700, or about 5,000. In another example, the lignin can have a MW of about 500 to about 30,000, about 1,000 to about 15,000, about 800 to about 6,000, about 2,000 to about 12,000, about 400 to about 10,000, or about 600 to about 8,000. In another example, the MW of the lignin can be about 600 to about 4,500, about 350 to about 1,100, about 750 to about 2,500, about 950 to about 3,100, about 1,500 to about 3,400, or about 1,800 to about 4,200.

The liquors from which the lignin can be recovered can also include one or more other constituents in addition to the lignin. For example, in the sulfite pulping process, the spent sulfite liquor can include lignosulfonates that can be present as salts of cations, such as magnesium, calcium, ammonium, sodium and/or other cations. The spent sulfite liquor solids can include about 40 wt % to about 65 wt % lignosulfonates with the remainder being carbohydrates and other organic and inorganic constituents dissolved in the liquor. Lignin products produced by other pulping processes can also include other materials such as carbohydrates, degradation products of carbohydrates, and resinous materials which are separated from the cellulosic materials with the lignin. It should be noted that it is not necessary to separate the lignin from the other constituents that can be present.

Suitable lignin material can include, but is not limited to, lignin in its native or natural state, e.g., non-modified or unaltered lignin, lignosulfonates, or any combination or mixture thereof. Suitable lignosulfonates can include, but are not limited to, ammonium lignosulfonate, sodium lignosulfonate, calcium lignosulfonate, magnesium lignosulfonate, or any combination or mixture thereof.

Suitable processes for isolating or otherwise separating lignin or lignin containing products form wood, plant, vegetable, or other lignin containing matter can include those discussed and described in U.S. Pat. Nos. 1,856,567; 2,525,433; 2,680,113; 2,690,973; 3,094,515; 3,158,520; 3,503,762; 3,585,104; 3,726,850; 3,769,272; 3,841,887; 4,100,016; 4,131,564; 4,184,845; 4,308,203; 4,355,996; 4,470,876; 4,740,591; and 4,764,596; U.S. Patent Application Publication No.: 2011/0294991; and WO Publication Nos. WO1992/018557A1, WO1993/021260A2; WO1994/024192A1; WO2005/062800A2; WO2006/031175A1; and WO2011/150508. Commercially available lignin can include, but is not limited to, lignosulfonates available from Tembec in Canada.

As used herein, the term “tannin” refers to both hydrolyzable tannins and condensed tannins. As such, the compound having at least two hydrogen atoms that are abstractable in the presence of hydroxyl radicals can be or include hydrolyzable tannins, condensed tannins, or a combination of hydrolyzable tannins and condensed tannins. Illustrative genera of shrubs and/or trees from which suitable tannins can be derived can include, but are not limited to, Acacia, Castanea, Vachellia, Senegalia, Terminalia, Phyllanthus, Caesalpinia, Quercus, Schinopsis, Tsuga, Rhus, Juglans, Carya, and Pinus, or any combination thereof. In another example, genera from which suitable tannins can be derived can include, but are not limited to, Schinopsis, Acacia, or a combination thereof. In another example, genera from which suitable tannins can be derived can include, but are not limited to, Pinus, Carya, or a combination thereof.

Hydrolyzable tannins are mixtures of simple phenols such as pyrogallol and ellagic acid and of esters of a sugar, e.g., glucose, with gallic and digallic acids. Illustrative hydrolyzable tannins can include, but are not limited to, extracts recovered from Castanea sativa, (e.g., chestnut), Terminalia and Phyllantus (e.g., myrabalans tree species), Caesalpinia coriaria (e.g., divi-divi), Caesalpinia spinosa, (e.g., tara), algarobilla, valonea, and Quercus (e.g., oak). Condensed tannins are polymers formed by the condensation of flavans. Condensed tannins can be linear or branched molecules. Illustrative condensed tannins can include, but are not limited to Acacia mearnsii (e.g., wattle or mimosa bark extract), Schinopsis (e.g., quebracho wood extract), Tsuga (e.g., hemlock bark extract), Rhus (e.g., sumach extract), Juglans (e.g., walnut), Carya illinoinensis (e.g., pecan), and Pinus (e.g., Radiata pine, Maritime pine, bark extract species).

The condensed tannins typically include about 70 wt % to about 80 wt % active phenolic ingredients (the “tannin fraction”) and the remaining ingredients (the “non-tannin fraction”) typically include, but are not limited to, carbohydrates, hydrocolloid gums, and amino and/or imino acid fractions. The condensed tannins can be used as recovered or extracted from the organic matter or the condensed tannins can be purified, e.g., about 95 wt % or more active phenolic ingredients. Hydrolyzable tannins and condensed tannins can be extracted from the starting material, e.g., trees and/or shrubs, using well established processes. A more detailed discussion of tannins is discussed and described in the Handbook of Adhesive Technology, Second Edition, CRC Press, 2003, chapter 27, “Natural Phenolic Adhesives I: Tannin,” and in Monomers, Polymers and Composites from Renewable Resources, Elsevier, 2008, chapter 8, “Tannins: Major Sources, Properties and Applications.”

The condensed tannins can be classified or grouped into one of two main categories, namely, those containing a resorcinol unit and those containing a phloroglucinol unit. Illustrative tannins that include the resorcinol unit include, but are not limited to, black wattle tannins and quebracho tannins. The resorcinol unit can be represented by Formula I below.

The resorcinol group is shown within the box overlaying the unit structure of black wattle and quebracho tannins in Formula II below. For simplicity, the structure of black wattle and quebracho tannins is represented by their flavonoid unit structure.

Illustrative tannins that include the phloroglucinol unit include, but are not limited to, pecan tannins and pine tannins. The phloroglucinol unit can be represented by Formula III below.

The phloroglucinol unit is shown within the box overlaying the unit structure of pecan and pine tannins in Formula IV below. For simplicity, the structure of pecan and pine tannins is represented by their flavonoid unit structure.

Phloroglucinol is known for higher reactivity than resorcinol. As such, tannins that include the phloroglucinol unit are more reactive than tannins that include the resorcinol unit.

If the binder composition includes a mixture of hydrolyzable tannins and condensed tannins any ratio with respect to one another can be used. For example, a binder composition that includes both hydrolyzable tannins and condensed tannins can have a concentration of condensed tannins of about 1 wt % to about 99 wt %, based on the combined weight of the hydrolyzable tannins and the condensed tannins. In another example, an binder composition that includes both hydrolyzable tannins and condensed tannins can have a concentration of condensed tannins of about 50 wt % or greater, about 55 wt % or greater, about 60 wt % or greater, about 70 wt % or greater, about 75 wt % or greater, about 80 wt % or greater, about 85 wt % or greater, about 90 wt % or greater, about 95 wt % or greater, or about 97 wt %, based on the combined weight of the hydrolyzable tannins and the condensed tannins.

If the binder composition includes two or more different tannins, the two or more tannins can have a resorcinol unit and/or a phloroglucinol unit. For example, the binder composition can include two different tannins that each include resorcinol units, e.g., quebracho tannins and black wattle tannins. In another example, the binder composition can include two different tannins, where a first tannin includes a resorcinol unit, e.g., black wattle tannin, and a second tannin includes a phloroglucinol unit, e.g., pine tannin. In another example, the binder composition can include two different tannins that each can independently include phloroglucinol units, e.g., pine tannins and pecan tannins.

The tannins can have an acidic pH. For example, the pH of the tannins can be of about 3, about 3.5, or about 4 to about 5, about 5.5, about 6, or about 6.5. The tannins can have resorcinol and/or phloroglucinol functional groups. Suitable, commercially available tannins can include, but are not limited to, black wattle tannin, quebracho tannin, hemlock tannin, sumac tannins, pecan tannin, mimosa tannin, pine tannins, or any mixture thereof.

The novolac resin can be produced by reacting a phenol component with an aldehyde component or aldehyde compound in the presence of an acid catalyst. The phenol component of the novolac resin can include a variety of substituted phenolic compounds, unsubstituted phenolic compounds, or any combination of substituted and/or unsubstituted phenolic compounds. For example, the phenol component can be phenol itself, i.e., monohydroxybenzene. Examples of substituted phenols can include, but are not limited to, alkyl-substituted phenols such as the cresols and xylenols; cycloalkyl-substituted phenols such as cyclohexyl phenol; alkenyl-substituted phenols; aryl-substituted phenols such as p-phenyl phenol; alkoxy-substituted phenols such as 3,5-dimethyoxyphenol; aryloxy phenols such as p-phenoxy phenol; and halogen-substituted phenols such as p-chlorophenol. Dihydric phenols such as catechol, resorcinol, hydroquinone, bisphenol A and bisphenol F also can also be used. Specific examples of suitable phenolic compounds (phenol components) for replacing a portion or all of the phenol used in preparing a novolac resin can include, but are not limited to, bisphenol A, bisphenol F, o-cresol, m-cresol, p-cresol, 3,5-5 xylenol, 3,4-xylenol, 3,4,5-trimethylphenol, 3-ethyl phenol, 3,5-diethyl phenol, p-butyl phenol, 3,5-dibutyl phenol, p-amyl phenol, p-cyclohexyl phenol, p-octyl phenol, 3,5 dicyclohexyl phenol, p-phenyl phenol, p-phenol, 3,5-dimethoxy phenol, 3,4,5-trimethoxy phenol, p-ethoxy phenol, p-butoxy phenol, 3-methyl-4-methoxy phenol, p-phenoxy phenol, naphthol, anthranol, substituted derivatives thereof, or any mixture thereof. In one example, about 80 wt % or greater, about 90 wt % or greater, or about 95 wt % or greater of the phenol component includes phenol (monohydroxybenzene).

Illustrative aldehyde compounds can include the so-called masked aldehydes or aldehyde equivalents, such as acetals or hemiacetals. Suitable aldehydes can be represented by the general formula R′CHO, where R′ can be a hydrogen or a hydrocarbyl group (e.g., a hydrocarbon radical) generally having 1 carbon atom to about 8 carbon atoms. Specific examples of suitable aldehyde compounds can include, but are not limited to, formaldehyde, acetaldehyde, propionaldehyde, butyraldehyde, furfuraldehyde, benzaldehyde, or any combination thereof. As used herein, the term “formaldehyde” can refer to formaldehyde, formaldehyde derivatives, other aldehydes, or combinations thereof. In one example, the aldehyde component can be formaldehyde. One or more difunctional aldehydes can also be used to produce the novolac resin, and could advantageously be used to introduce cross-links ultimately into the at least partially cured novolac resin.

The aldehyde can be used in many forms such as solid, liquid, and/or gas. Considering formaldehyde in particular, the formaldehyde can be or include paraform (solid, polymerized formaldehyde), formalin solutions (aqueous solutions of formaldehyde, sometimes with methanol, in about 37 wt %, about 44 wt %, or about 50 wt % formaldehyde concentrations), Urea-Formaldehyde Concentrate (“UFC”), and/or formaldehyde gas in lieu of or in addition to other forms of formaldehyde can also be used. In another example, the aldehyde can be or include a pre-reacted urea-formaldehyde mixture having a urea to formaldehyde weight ratio of about 1:2 to about 1:3.

A molar ratio of formaldehyde to phenol used to produce the novolac resin can be about 0.5 to about 0.95 or about 0.7 to about 0.85. The reaction between the phenol and the formaldehyde to produce the novolac resin can be carried out in the presence of an acid catalyst under acidic conditions. Suitable acid catalysts can include, but are not limited to, oxalic acid, sulfuric acid, p-toluene sulfuric acid, hydrochloric acid, salicylic acid, mineral acids and salts thereof, or any combination thereof. Mixed catalyst systems, such as ZnOAc/oxalic acid and other divalent metal compounds, e.g., acetates, can be used to prepare “high-ortho” novolac resins. Divalent metal compounds can include Ca, Mg, Zn, Cd, Pb, Cu, Co, and Ni. In some examples, catalysts can include oxalic acid, sulfuric acid, p-toluenesulfonic acid, or ZnOAc/oxalic acid. In one specific example, the catalyst can be oxalic acid or ZnOAc/oxalic acid.

The amount of acid catalyst used to produce the novolac resin can be sufficient to catalyze the reaction between the phenol and formaldehyde to produce the novolac resin. The phenol/formaldehyde reaction can be conducted in about 1 hour to about 6 hours, e.g., about 2 hours to about 4 hours. The phenol/formaldehyde reaction can be carried out at a temperature of about 80° C. to about 100° C., e.g., about 95° C. to about 100° C. The reaction can be carried out at atmospheric pressure, although increased pressure can be utilized to permit the application of higher temperatures and, therefore, faster reaction rates and accordingly shorter reaction times.

The novolac resin can be treated to remove water and/or other volatile organic materials by heating, such as by distillation. After this treatment, the free phenol can be about 0.001 wt % to about 2 wt %, or about 0.001 wt % to about 0.5 wt %. Distillation of the resulting novolac resin can be performed at atmospheric pressure by heating to about 140° C., and then under a vacuum until the resin reaches a temperature of about 180° C. to about 220° C. Other suitable methods for treating the resin via heat can include thin-film evaporators. The resulting molten novolac resin can be cooled to a temperature of less than 100° C.

If desired, the novolac resin can be neutralized. Neutralization of the novolac resin can be accomplished by the addition of one or more bases or base compounds, such as sodium hydroxide and/or potassium hydroxide, or its equivalent. The base compound can be added in an amount sufficient to raise the pH of the novolac resin to about 5 to about 9, e.g., about 6 to about 8. Typically, about 10 wt % to about 30 wt % of water, based on the total resin solids, can be added. Suitable novolac resins and inverted novolac resins can be as discussed and described in U.S. Pat. No. 5,670,571 and U.S. Patent Application Publication No. 2008/0280787.

The modified phenol formaldehyde resin can be or include ARYLZENE®, which can be represented by the general Formula V:

Other illustrative modified phenol formaldehyde resins can be or include those discussed and described in U.S. Pat. Nos. 5,674,970; 5,739,259; 5,756,642; 5,756,655; 5,770,750; 5,773,552; 5,837,798; 5,889,137; 6,166,151; 6,291,077; 6,399,740; and 6,569,953.

If the bisphenol can be present as or as a component of the polyphenolic compound, any polyphenolic bisphenol compound can be used. Illustrative bisphenols can include, but are not limited to, bisphenol A, bisphenol B, bisphenol C, bisphenol E, bisphenol F, bisphenol G, or any mixture thereof.

Humic acid can be represented by the general Formula VI:

Any one or more of the polyphenolic compounds can be modified with one or more compounds having one or more carbon-carbon double bonds and one or more reactive functional groups. For example, the mixture can include one or more polyphenolic compounds modified by at least partially reacting with one or more unsaturated monomers having one or more reactive functional groups. Any suitable compounds having one or more carbon-carbon double bonds and one or more reactive functional groups or combination of compounds having one or more carbon-carbon double bonds and one or more reactive functional groups can be used to produce the modified polyphenolic compounds. The compounds having one or more carbon-carbon double bonds and one or more reactive functional groups can be nonionic. Illustrative compounds having one or more carbon-carbon double bonds and one or more reactive functional groups can include, but are not limited to, one or more unsaturated glycidyl ethers, one or more unsaturated glycidyl esters, one or more unsaturated mono-epoxides, one or more unsaturated methylol compounds, maleic anhydride, or any mixture thereof.

Illustrative unsaturated glycidyl ethers can be represented by general Formula VII:

where R¹ can be an ethylenically unsaturated radical such as vinyl, allyl, alkenyl, and the like. Suitable glycidyl ethers can include, but are not limited to, vinyl glycidyl ether, isopropenyl glycidyl ether, oleyl glycidyl ether, allyl glycidyl ether, p-vinylbenzyl glycidyl ether, o-allyl phenyl glycidyl ether, butenyl glycidyl ether, 4-vinylcyclohexyl glycidyl ether, abietylglycidyl ether, cyclohexeneylmethyl glycidyl ether, methallyl glycidyl ether, or any combination thereof.

Illustrative unsaturated glycidyl esters can be represented by general Formula VIII:

where R² can be an unsaturated, unsubstituted alkyl radical having 2 carbon atoms to about 19 carbon atoms. Suitable glycidyl esters can include, but are not limited to, glycidyl methacrylate, glycidyl acrylate, glycidyl crotonate, glycidyl oleate, diglycidyl maleate, diglycidyl fumarate, or any combination thereof.

Illustrative unsaturated mono-epoxides can include, but are not limited to, linear or cycloaliphatic epoxy compounds, where the unsaturation is terminal. Suitable unsaturated mono-epoxides can be represented by general Formula IX:

where R³ can be a single bond or an alkylene optionally containing alkyl pendant groups; R⁴, R⁵, and R⁶ can independently be hydrogen, alkyl (straight, branched or cyclic), or any two of R⁴, R⁵, or R⁶ can be alkylene and combined to form a 5 to 12 carbon cyclic ring, optionally containing alkyl pendants; and the number of carbon atoms in R³, R⁴, R⁵, and R⁶ can be such that the total number of carbon atoms in the epoxide can be about 4 carbon atoms to about 50 carbon atoms. Suitable unsaturated mono-epoxides can include, but are not limited to, 4-vinyl cyclohexene oxide, 1-methyl-4-isopropenyl cyclohexene monoxide, butadiene monoxide, or any combination thereof.

Illustrative unsaturated methylol compounds can be represented by the general Formula X:

where R⁷, R⁸, R⁹, and R¹⁰ can independently be hydrogen or a hydrocarbyl group, e.g., an alkyl group, containing 1 carbon atom to about 6 carbon atoms. For example, an alkyl group can include 1 carbon atom to about 4 carbon atoms. In at least one example, R⁷, R⁸, R⁹, and R¹⁰ can each independently be methyl or hydrogen. Suitable unsaturated methylol compounds can include, but are not limited to, N-methylol acrylamide, N-methylol methacrylamide, N-methylol crotonamide, or any combination thereof. The N-methylol ethylenically unsaturated amide can be in the form of an aqueous solution.

In at least one example, the modified polyphenolic compounds can be completely free, essentially free, or substantially free of any anionic monomers. For example, the modified polyphenolic compounds can contain less than 3 wt %, less than 2.5 wt %, less than 2 wt %, less than 1.5 wt %, less than 1 wt %, less than 0.7 wt %, less than 0.5 wt %, less than 0.3 wt %, less than 0.1 wt %, less than 0.05 wt %, or less than 0.01 wt % anionic monomers. In at least one example, the modified polyphenolic compounds can be free or essentially free of any ionic monomers. For example, the modified polyphenolic compounds can contain less than 3 wt %, less than 2.5 wt %, less than 2 wt %, less than 1.5 wt %, less than 1 wt %, less than 0.7 wt %, less than 0.5 wt %, less than 0.3 wt %, less than 0.1 wt %, less than 0.05 wt %, or less than 0.01 wt % ionic monomers. In at least one other example the modified polyphenolic compounds can be free or essentially free of any anionic and ionic monomers. For example, the modified polyphenolic compounds can contain less than 3 wt %, less than 2.5 wt %, less than 2 wt %, less than 1.5 wt %, less than 1 wt %, less than 0.7 wt %, less than 0.5 wt %, less than 0.3 wt %, less than 0.1 wt %, less than 0.05 wt %, or less than 0.01 wt % anionic and ionic monomers. As used herein, the terms “essentially free of anionic monomers” and “essentially free of ionic monomers” means the modified polyphenolic compounds does not include any intentionally added anionic monomers or ionic monomers, respectively. Said another way, the terms “essentially free of anionic monomers” and “essentially free of ionic monomers” means the modified polyphenolic compounds may include anionic monomers and/or ionic monomers present as an impurity. Suitable modified polyphenolic compounds and methods for making same can be as discussed and described in U.S. Patent Application Publication No. 2013/0287993.

If two or more polyphenolic compounds are present, the two or more polyphenolic compounds can be present in any amount with respect to one another. For example, if the polyphenolic compound includes a first polyphenolic compound and a second polyphenolic compound, the first polyphenolic compound can be present in an amount of about 1 wt % to about 99 wt % and, conversely the second polyphenolic compound can be present in an amount of about 99 wt % to about 1 wt, based on the combined weight of the polyphenolic compound. In another example, the amount of the first polyphenolic compound can be of about 5 wt %, about 10 wt %, about 15 wt %, about 20 wt %, about 25 wt % about 30 wt %, about 35 wt %, about 40 wt %, or about 45 wt % to about 60 wt %, about 65 wt %, about 70 wt %, about 75 wt %, about 80 wt %, about 85 wt %, about 90 wt %, or about 95 wt %, based on the total weight of the first and second polyphenolic compounds.

In one or more embodiments, the unsaturated compound can include, but is not limited to, dicyclopentadiene (DCPD), 4-vinylcyclohexene, one or more vinyl ethers, one or more allyl ethers, diallyl phthalate, allyl crotonate, allyl cinamate, allyl methacrylate, vinyl methacrylate, ethylene glycol diacrylate, ethylene glycol dimethacrylate, diethylene glycol diacrylate, diethylene glycol dimethacrylate, poly(ethylene glycol)diacrylate, poly(ethylene glycol)dimethacrylate, trimethylolpropane triacrylate (TMPTA), pentaerythritol tetraacrylate, pentaerythritol triacrylate, polyacrylate, one or more conjugated dienes, one or more terpenes, one or more drying oils having an iodine number of about 115 or greater, one or more unsaturated prepolymers, one or more polyesters with one or more incorporated vinyl unsaturations, styrene-butadiene rubber (SBR), one or more starches having at least one unsaturated and polymerizable olefinic group, polymers derived from ring-opening polymerization of allyl caprolactone, a product or products formed by reacting one or more polyamidoamines and one or more unsaturated glycidyl ethers, or any mixture thereof.

In one or more embodiments, the unsaturated compound can have a double bond equivalent molecular weight of about 33, about 50, about 100, about 150, about 200, about 500, about 1,000, about 5,000, about 10,000, or about 15,000 to about 50,000, about 75,000, about 100,000, about 150,000, about 200,000, or about 250,000. In one or more embodiments, the unsaturated compound can have a double bond equivalent molecular weight of at least 33, at least 40, at least 45, at least 50, at least 75, at least 100, at least 200, at least 300, at least 400, at least 500, at least 1,000, at least 2,500, at least 5,000, at least 10,000, at least 20,000, at least 30,000, at least 40,000, at least 50,000, at least 60,000, at least 70,000, at least 80,000, at least 90,000, at least 100,000, at least 110,000, at least 120,000, at least 130,000, at least 140,000, or at least 150,000 to about 175,000, about 200,000, about 225,000, or about 250,000.

As used herein, the double bond equivalent molecular weight can be calculated by dividing the molecular weight of the unsaturated compound by the number of carbon-carbon double bonds the unsaturated compound contains. For example, if the unsaturated compound is cyclopentadiene, which has a molecular weight of 66.1 g/mol and two carbon-carbon double bonds, the double bond equivalent molecular weight is 33.05 (66.1 divided by 2). Accordingly, as used herein, the term “unsaturated compound” includes compounds that can be considered a monomer or discrete molecules. In another example, if the unsaturated compound is trimethylolpropane triacrylate (TMPTA), which has a molecular weight of 296.32 g/mol and 3 carbon-carbon double bonds, the double bond equivalent molecular weight 98.8.

In one or more embodiments, the unsaturated compound can have a weight average molecular weight (Mw) of about 200, about 250, about 300, about 350, about 400, about 450, about 500, about 550, about 600, or about 650 to about 1,000, about 1,500, about 2,000, about 2,500, about 3,000, about 3,500, about 4,000, about 4,500, or about 5,000. For example, the unsaturated compound can have a weight average molecular weight of about 300 to about 3,000, about 330 to about 770, about 380 to about 930, about 470 to about 1,150, about 700 to about 1,800, about 800 to about 2,200, about 1,200 to about 2,00, about 400 to about 2,800, about 500 to about 2,700, about 600 to about 2,600, or about 700 to about 2,500. In one or more embodiments, the unsaturated compound can have a weight average molecular weight of at least 300, at least 325, at least 350, at least 375, at least 400, at least 425, at least 450, at least 475, at least 500, at least 525, at least 550, at least 575, at least 600, at least 625, at least 650, at least 675, at least 700, at least 750, at least 775, at least 800, at least 825, at least 850, at least 875, at least 900, at least 925, at least 950, at least 975, or at least 1,000.

Illustrative vinyl aromatic compounds can include, but are not limited to, 2-allylphenol, 4-allylphenol, and a mixture thereof. Illustrative vinyl ethers can include, but are not limited to, triethyleneglycol divinyl ether, divinyl ether, or a mixture thereof. Illustrative allyl ethers can include, but are not limited to, diallyl ether, trimethylolpropane diallyl ether, triallyl cyanurate, or any mixture thereof. Illustrative conjugated dienes can include, but are not limited to, 1,3-butadiene, 2,3-dimethylbutadiene, 2-methyl-1,3-butadiene (isoprene), 1,3-pentadiene (piperylene), cyclopentadiene, 2-chloro-1,3-butadiene (chloroprene), or any mixture thereof. Illustrative terpenes can include, but are not limited to, sesquiterpenes, or any mixture thereof. Illustrative sesquiterpenes can include, but are not limited to, farnesene, or any mixture thereof. Illustrative one or more drying oils having an iodine number of about 115 or greater can include, but are not limited to, linseed oil, soybean oil, sunflower oil, tung oil, grape seed oil, wheat germ oil, corn oil, or any mixture thereof. In some example, the drying oil can have an iodine number of about 115 to about 180 or greater. Illustrative unsaturated prepolymers can include, but are not limited to, unsaturated polyester prepolymers, unsaturated polyether prepolymers, unsaturated polyamide prepolymers, unsaturated polyurethane prepolymers, or any mixture thereof. Illustrative polyesters with one or more incorporated vinyl unsaturations can include, but are not limited to, methacrylate, acrylate modified or terminated polyesters, or any mixture thereof.

As noted above, the α,β-unsaturated carbonyl compound can be, but is not limited to, an α,β-unsaturated aldehyde (e.g., an enal), an α,β-unsaturated ketone (e.g., an enone), an α,β-unsaturated carboxylic acid, an α,β-unsaturated ester, an α,β-unsaturated amide, an α,β-unsaturated acyl halide, an α,β-unsaturated acid anhydride, or an α,β-unsaturated imide. Illustrative α,β-unsaturated carbonyl aldehydes can include, but are not limited to, crotonaldehyde, 3-methylcrotonaldehyde, methacrolein, tiglic aldehyde, isomers thereof, or any mixture thereof. Illustrative α,β-unsaturated ketones can include, but are not limited to, methyl vinyl ketone, ethyl vinyl ketone, isomers thereof, or any mixture thereof. Illustrative α,β-unsaturated carboxylic acids can include, but are not limited to, maleic acid, itaconic acid, fumaric acid, glutaconic acid, citraconic acid, traumatic acid, muconic acid, aconitic acid, isomers thereof or any mixture thereof. Illustrative α,β-unsaturated esters can include, but are not limited to, esters of maleic acid, itaconic acid, fumaric acid, glutaconic acid, citraconic acid, traumatic acid, muconic acid, aconitic acid, isomers thereof, or any mixture thereof. An illustrative α,β-unsaturated amide can include, but are not limited to, acrylamide. Illustrative α,β-unsaturated acyl halides can include, but are not limited to, acryloyl chloride, methacryloyl chloride, crotonoyl chloride, fumaryl chloride, itaconyl chloride, sorbic chloride, isomers thereof, or any mixture thereof. An illustrative α,β-unsaturated acid anhydride can include, but is not limited to, maleic anhydride, an isomer thereof, or a mixture thereof. An illustrative α,β-unsaturated imide can include, but is not limited to, maleimide, an isomer thereof, or a mixture thereof.

Other compounds having one or more pi-bonds (e.g., unsaturated bonds) that is capable of going through a radical chain reaction mechanism, but is also conjugated with an aromatic moiety, can include, but are not limited to, vinyl aromatics, such as styrene, methylstyrenes, vinyl toluene, vinyl naphthalene, divinylbenzene (DVB), and vinylpyridine; methylstyrenes such as α-methylstyrene, trans-β-methylstyrene; and any mixture thereof.

Illustrative unsaturated starch compounds having at least one unsaturated and polymerizable olefinic group can be represented by Formula XI below.

where R¹¹ can be hydrogen or an alkyl group. Suitable starches can include, but are not limited to, maize or corn, waxy maize, high amylose maize, potato, tapioca, and wheat starch. Other starches such as genetically engineered starches can include high amylose potato and potato amylopectin starches. Suitable methods for preparing unsaturated starch compounds having at least one unsaturated and polymerizable olefinic group can include those discussed and described in U.S. Pat. No. 2,668,156.

The unsaturated prepolymer can include one or more monounsaturated prepolymers, one or more polyunsaturated prepolymers, or any mixture thereof. In one or more embodiments, suitable polyunsaturated prepolymers can include at least two sites of unsaturation, at least three sites of unsaturation, at least 4 sites of unsaturation, at least 5 sites of unsaturation, at least 6 sites of unsaturation, or more. In one or more embodiments, the unsaturated prepolymer can be unsaturated polyester prepolymers, unsaturated polyether prepolymers, unsaturated polyamide prepolymers, unsaturated polyurethane prepolymers, or any mixture thereof.

The unsaturated polyester prepolymer can be synthesized or produced by reacting one or more polyacids and one or more polyols with one another. For example, the unsaturated prepolymer can be produced via monoester formation. In another example, the unsaturated polyester prepolymer can be produced by reacting the polyacid and the polyol via a condensation reaction. As used herein, the term “polyacid” refers to compounds having at least two reactive acid groups per molecule. The acid functionality can be a carboxylic acid, a sulfonic acid, or a combination thereof. The term “polyacid” can also refer to acid anhydrides, e.g., maleic anhydride. The term “polyacid” can also refer to compounds containing at least one acid group per molecule and at least one acid anhydride group per molecule, e.g., a maleated fatty acid. As used herein, the term “polyol” refers to compounds that contain two or more hydroxyl functional groups.

In one or more embodiments, the one or more sites of unsaturation in the unsaturated polyester prepolymer can be directly introduced from the polyacid and/or the polyol, e.g., at least one of the polyacid and the polyol can include one or more sites of unsaturation. Said another way, the unsaturated polyester prepolymer can be produced by reacting one or more unsaturated polyacids with one or more saturated polyols, reacting one or more unsaturated polyols with one or more saturated polyacids, and/or by reacting one or more unsaturated polyacids with one or more unsaturated polyols. In one or more embodiments, the sites of unsaturation in the unsaturated polyester prepolymer can be appended to an initial prepolymer formed by reacting the polyacid and the polyol with one or more unsaturated compounds. In another example, the unsaturation sites of the unsaturated polyester prepolymer can be introduced via at least one of the polyol and the poly acid, and an additional unsaturated compound. Illustrative additional unsaturated compounds can include, but are not limited to, unsaturated alcohols, unsaturated acids, unsaturated epoxides, or any mixture thereof.

The polyacid and polyol components can be mixed, blended, or otherwise combined with one another to produce a reaction mixture. The polyacid and polyol can be reacted under conditions sufficient to substantially react the primary hydroxyl groups of the polyol with the polyacid, but insufficient to cause reaction of the secondary hydroxyl groups of the polyol with the polyacid to a substantial extent. As used herein, the phrase “substantially react the primary hydroxyl groups of the polyol with the polyacid” means that at least 90% of the primary hydroxyl groups of the polyol are reacted with the polyacid. As used herein, the phrase “insufficient to cause reaction of the secondary hydroxyl groups of the polyol with the polyacid to a substantial extent” means that less than 10% of the secondary hydroxyl groups of the polyol are reacted with the polyacid. For example, the polyacid and the polyol can be combined in a reaction vessel or container and heated to a temperature of about 50° C., about 60° C., about 70° C., or about 80° C. to about 110° C., about 125° C., about 140° C., or about 155° C. In another example, the polyacid and the polyol can be heated to a temperature of about 60° C. to about 130° C., about 80° C. to about 115° C., about 100° C. to about 150° C., or about 75° C. to about 135° C. The polyacid and the polyol can be reacted with one another for a time of about 10 minutes, about 30 minutes, about 1 hour, or about 2 hours to about 4 hours, about 6 hours, about 8 hours, or about 10 hours.

The progress of the reaction between the polyacid and the polyol can be monitored via any suitable method. One method for monitoring the extent of the reaction between the polyacid and the polyol can be through the use of infrared spectroscopy. For example, infrared spectroscopy can detect the presence of any unreacted polyacid. In one example, the reaction between the polyacid and the polyol can be carried out until the presence of the polyacid is no longer detected. It should be noted, however, that the unsaturated polyester prepolymer can include unreacted polyacid and/or unreacted polyol.

The polyacid and the polyol can be combined with one another in any desired ratio. For example, the polyol and the polyacid can be combined with one another at a molar ratio raging of about 1:5, about 1:4, or about 1:2, to about 1:1, about 2:1, about 4:1, or about 6:1. In at least one example, the amount of the polyacid combined with the polyol can be sufficient to provide a ratio of reactive acid and/or anhydride groups to hydroxyl groups of about 1:1 to about 2:1. In one or more embodiments, for each hydroxyl group present in the polyol about 1 acid group, about 2 acid groups, or about 3 acid groups can be present in the mixture of the polyol and the polyacid.

The polyacid can be or include, but is not limited to, one or more unsaturated and/or saturated aliphatic polyacids, one or more aromatic polyacids, one or more cyclo-aliphatic polyacids, one or more acid anhydrides, or any mixture thereof. Suitable unsaturated aliphatic diacids and saturated aliphatic diacids can include about 2 carbon atoms to about 12 carbon atoms, about 3 carbon atoms to about 10 carbon atoms, or about 4 carbon atoms to about 8 carbon atoms. Illustrative unsaturated aliphatic diacids can include, but are not limited to, maleic acid, itaconic acid, fumaric acid, glutaconic acid, citraconic acid, traumatic acid, muconic acid, aconitic acid, or any mixture thereof. Illustrative saturated aliphatic diacids can include, but are not limited to, oxalic acid, malonic acid, succinic acid, glutaric acid, adipic acid, pimelic acid, suberic acid, azelaic acid, sebacic acid, or any combination or mixture thereof. Illustrative aromatic diacids can include, but are not limited to, phthalic acid, isophthalic acid, terephthalic acid, or any combination or mixture thereof. Illustrative cyclo-aliphatic diacids can include, but are not limited to, cyclobutanedicarboxylic acid, cyclopentanedicarboxylic acid, cyclohexanedicarboxylic acid, isomers thereof, or any combination or mixture thereof. Illustrative acid anhydrides can include, but are not limited to, phthalic anhydride, mellitic anhydride, pyromellitic anhydride, maleic anhydride, or any combination or mixture thereof. In one or more embodiments, the polyacid can also include one or more unsaturated fatty acids reacted with any one or more of the polyacids discussed and described above. For example, the polyacid can be or include the Alder-ene reaction product between one or more unsaturated fatty acids and maleic anhydride, e.g., the polyacid can be or include one or more maleated fatty acids.

Illustrative saturated polyols can include, but are not limited to, ethylene glycol, polyglycerol, hyperbranched polyglycerol, diethylene glycol, triethylene glycol, polyethylene oxide (hydroxyl terminated), glycerol, pentaerythritol, trimethylolpropane, diethanolamine, triethanolamine, ethyl diethanolamine, methyl diethanolamine, sorbitol, monosaccharides, such as glucose and fructose, disaccharides, such as sucrose, and higher polysaccharides such as starch and reduced and/or modified starches, dextrin, maltodextrin, polyvinyl alcohols, hydroxyethylcellulose, 1,4-cyclohexane diol, or any combination or mixture thereof. Illustrative unsaturated polyols can include, but are not limited to, 2-butene-1,4-diol; hydroxyl-terminated polybutadiene (HTPB); or any combination or mixture thereof.

Illustrative unsaturated alcohols suitable for introducing, appending, or otherwise providing one or more sites of unsaturation in the unsaturated polyester prepolymer can include, but are not limited to, any one or more of the unsaturated polyols discussed and described above, allylic alcohols, unsaturated alcohols obtained via metathesis reaction of hydroxyl-substituted unsaturated fatty acid or fatty acid esters, or any combination or mixture thereof. The preparation of unsaturated alcohols via metathesis reaction can be as discussed and described in U.S. Pat. No. 7,176,336. Illustrative unsaturated acids suitable for introducing, appending, or otherwise providing one or more sites of unsaturation in the unsaturated polyester prepolymer can include, but are not limited to, any one or more of the unsaturated polyacids discussed and described above, or any combination or mixture thereof. Suitable unsaturated epoxides suitable for introducing, appending, or otherwise providing one or more sites of unsaturation in the unsaturated polyester prepolymer can include, but are not limited to, allyl glycidyl ether; 3,4-epoxy-1-butene; 1,2-epoxy-5-hexene; any combination thereof or mixture thereof.

In one or more embodiments, one or more catalysts or unsaturated polyester prepolymer catalysts can optionally be present when the polyacid and the polyol are reacted with one another. Suitable catalysts can include, but are not limited to, monobutyltin oxide, dibutyltin oxide, dibutyltin dilaurate, or any mixture thereof. The one or more catalysts, if present, can be present in an amount of about 0.05 wt %, about 0.1 wt %, about 0.5 wt %, or about 1 wt % to about 2 wt %, about 3 wt %, about 4 wt %, or about 5 wt %, based on the combined weight of the polyacid and the polyol.

In one or more embodiments, the unsaturated polyester prepolymer can be combined with one or more reactive monomers in lieu of or in addition to the water. Illustrative reactive monomers that can be combined with the unsaturated polyester prepolymer can include, but are not limited to, styrene, methyl styrene, chlorostyrene, vinyl toluene, divinyl benzene, vinyl acetate, acrylic acid, methacrylic acid, lower alkyl esters of acrylic acid, lower alkyl esters of methacrylic acid, diallyl phthalate, vegetable oils, e.g., linseed oil, soy bean oil, sunflower oil, tung oil, or any combination or mixture thereof. If the unsaturated polyester prepolymer is combined with one or more reactive monomers, the amount of the one or more reactive monomers can be of about 1 wt %, about 5 wt %, about 10 wt %, about 15 wt %, or about 20 wt % to about 40 wt %, about 45 wt %, about 50 wt %, about 55 wt %, or about 60 wt %, based on the combined weight of the one or more reactive monomers and the unsaturated polyester prepolymer.

The unsaturated polyamide prepolymers can be produced by reacting one or more polyamines with one or more polyacids. The unsaturated polyamide prepolymers can also be produced by reacting one or more polyamines with one or more esters. In one or more embodiments, the one or more sites of unsaturation in the unsaturated polyamide prepolymer can be directly introduced from the polyacid and/or the polyamine, e.g., at least one of the polyacid and the polyamine can include one or more sites of unsaturation. Said another way, the unsaturated polyamide prepolymer can be produced by reacting one or more unsaturated polyacids with one or more saturated polyamines, reacting one or more unsaturated polyamines with one or more saturated polyacids, and/or by reacting one or more unsaturated polyacids with one or more unsaturated polyamines. In one or more embodiments, the sites of unsaturation in the unsaturated polyamide prepolymer can be appended to an initial prepolymer formed by reacting the polyacid and the polyamine with one or more unsaturated compounds. In another example, the unsaturation sites of the unsaturated polyamide prepolymer can be introduced via at least one of the polyamine and the poly acid, and an additional unsaturated compound. Illustrative additional unsaturated compounds can include, but are not limited to, unsaturated alcohols, unsaturated acids, unsaturated epoxides, or any mixture thereof.

The polyacid and polyamine components can be mixed, blended, or otherwise combined with one another to produce a reaction mixture. The reaction mixture can be reacted under conditions sufficient to react the polyacid with the polyamine to produce the unsaturated polyamide prepolymer. For example, the polyacid and the polyamine can be combined in a reaction vessel or container and heated to a temperature of about 50° C., about 60° C., about 70° C., or about 80° C. to about 110° C., about 125° C., about 140° C., or about 155° C. In another example, the polyacid and the polyamine can be heated to a temperature of about 60° C. to about 130° C., about 80° C. to about 115° C., about 100° C. to about 150° C., or about 75° C. to about 135° C. The polyacid and the polyamine can be reacted with one another for a time of about 10 minutes, about 30 minutes, about 1 hour, or about 2 hours to about 4 hours, about 6 hours, about 8 hours, or about 10 hours. Polyamides can also be produced or made via transamidation.

The progress of the reaction between the polyacid and the polyamine can be monitored via any suitable method. One method for monitoring the extent of the reaction between the polyacid and the polyamine can be through the use of infrared spectroscopy. For example, infrared spectroscopy can detect the presence of any unreacted polyacid. In one example, the reaction between the polyacid and the polyamine can be carried out until the presence of the polyacid is no longer detected. It should be noted, however, that the unsaturated polyamide prepolymer can include unreacted polyacid and/or unreacted polyamine.

The polyacid and the polyamine can be combined with one another in any desired ratio. For example, the polyamine and the polyacid can be combined with one another at a molar ratio raging of about 1:5, about 1:4, or about 1:2, to about 1:1, about 2:1, about 4:1, or about 6:1. In at least one example, the amount of the polyacid combined with the polyamine can be sufficient to provide a ratio of reactive acid and/or anhydride groups to amine groups of about 1:1 to about 2:1. For example, for each amine group present in the polyamine, 1 acid group, 2 acid groups, or 3 acid groups can be present in the mixture of the polyamine and the polyacid.

Suitable polyacids can include those discussed and described above or elsewhere herein. Illustrative saturated polyamines can include, but are not limited to, ethylenediamine, propylenediamine, hexamethylenediamine, diethylenetriamine (DETA), triethylenetetramine (TETA), tetraethylenepentamine (TEPA), 1,3-propanediamine, 1,4-butanediamine, hyperbranched polyethyleneimine, or any combination or mixture thereof. Illustrative unsaturated polyamines can include those represented by the following general Formula XII below:

where R¹² and R¹³ can independently be an organic group having 1 carbon atom to about 24 carbon atoms, e.g., an alkyl group containing 1 carbon atom to about 12 carbon atoms, and n can be an integer of 2 to about 12. Illustrative unsaturated polyamines having Formula XII can be prepared according to the methods discussed and described in U.S. Pat. No. 3,773,833.

The unsaturated polyether prepolymers can be produced by polymerization of allyl glycidyl ether (AGE) to form poly(allyl glycidyl ether) (PAGE). Resulted prepolymer can have pendant allyl groups. Suitable reaction conditions for producing the unsaturated polyurethane prepolymer can include those discussed and described in Lee, B. F. et al., “Poly(allyl Glycidyl Ether)—A Versatile and Functional Polyether Platform,” Journal of Polymer Science Part A: Polymer Chemistry, Vol. 49, August 2011, pp. 4498-4504. The copolymerization reaction of AGE with other monomers can be as discussed and described in Sunder, A. et al., “Copolymers of Glycidol and Glycidyl Ethers: Design of Branched Polyether Polyols by Combination of Latent Cyclic AB₂ and ABR Monomers,” Macromolecules, Vol. 33, September 2000, pp. 7682-7692, and Erberich, M. et al., “Polyglycidols with Two Orthogonal Protective Groups: Preparation, Selective Deprotection, and Functionalization,” Macromolecules, Vol. 40, April 2007, pp. 3070-3079.

The unsaturated polyurethane prepolymers can be produced by reacting one or more polyisocyanates with one or more compounds having active hydrogen functionality. Moieties that provide active hydrogen functionality can include, but are not limited to, hydroxyl groups, mercaptan groups, amine groups, and carboxyl groups. In some examples, hydroxyl groups can be used as a compound having active hydrogen functionality.

Suitable polyisocyanates can include, but are not limited to, hexamethylene diisocyanate, toluene diisocyanate (TDI), diphenylmethane diisocyanate (MDI), m-phenylene and p-phenylene diisocyanates, bitolylene diisocyanate, cyclohexane diisocyanate (CHDI), bis-(isocyanatomethyl)cyclohexane (H₆XDI), dicyclohexylmethane diisocyanate (HOMO, dimer acid diisocyanate (DDI), trimethyl hexamethylene diisocyanate, lysine diisocyanate and its methyl ester, methyl cyclohexane diisocyanate, 1,5-napthalene diisocyanate, xylylene and xylene diisocyanate and methyl derivatives thereof, polymethylene polyphenyl isocyanates, chlorophenylene-2,4-diisocyanate, polyphenylene diisocyanates available commercially as, for example, Mondur MR or Mondur MRS, isophorone diisocyanate (IPDI), hydrogenated methylene diphenyl isocyanate (HMDI), tetramethyl xylene diisocyanate (TMXDI), hexamethylene diisocyanate (HDI), or oligomer materials of these materials such as a trimer of IPDI, HDI or a biuret of HDI, and the like, and mixtures thereof. Triisocyanates and high-functional isocyanates can also be used. Aromatic and aliphatic diisocyanates, for example, biuret and isocyanurate derivatives can be used.

Suitable polyols for reacting with the polyisocyanates can include, but are not limited to, polyether polyols (e.g., block polyethylene and polypropylene oxide homo- and copolymers ranging in molecular weight of about 300 to about 3,000), alkylated polyols (e.g., polytetramethylene ether glycols), caprolactone-based polyols, and the like. In one or more embodiments, the reactants for making the polyurethane prepolymer can be or include mixtures of aliphatic and aromatic polyols, or a multi-functional, active hydrogen-bearing polymer. As such, in addition to or in lieu of polyether polyols, the hydroxyl-functional component can include derivatives of acrylates, esters, vinyls, and castor oils, as well as polymers, or any mixture thereof.

Isocyanate equivalents can predominate over active hydrogen equivalents in the polyisocyanate/polyol reaction mixture to produce a prepolymer that can include residual isocyanate groups. The isocyanate and the polyol can be combined with one another in any desired ratio. For example, the isocyanate and the polyol can be combined with one another at a molar ratio raging of about 1:5, about 1:4, or about 1:2, to about 1:1, about 2:1, about 4:1, or about 5:1. Suitable reaction conditions for producing the unsaturated polyurethane prepolymer can include those discussed and described in Heiss, et al., “Influence of Acids and Bases on Preparation of Urethane Polymers,” Industrial and Engineering Chemistry, Vol. 51, No. 8, August 1959, pp. 929-934. Depending upon the reaction conditions used (such as, for example, temperature and the presence of strong acids or bases, and catalysts), the reaction may lead to the formation of ureas, allophanates, biurets, or isocyanates.

Suitable amine group containing compounds that can be reacted with the polyisocyanates can include, but are not limited to, unsaturated polyamines represented by the general Formula XII discussed and described above. Suitable carboxyl group containing compounds that can be reacted with the polyisocyanates can include, but are not limited to, unsaturated aliphatic diacids. Illustrative unsaturated aliphatic diacids can include, but are not limited to, maleic acid, itaconic acid, fumaric acid, glutaconic acid, citraconic acid, traumatic acid, muconic acid, aconitic acid, or any mixture thereof.

Polyamidoamines and unsaturated glycidyl ethers suitable for producing one or more products formed by reacting the polyamidoamine and the unsaturated glycidyl ether can widely vary. The polyamidoamine can be a reaction product of a polyamine and a dicarboxylic acid. In some example, the polyamine can be dimethylenetriamine, diethylenetriamine, triethylenetetramine, tripropylenetetramine, tetraethylenepentamine, pentaethylenehexamine, or any mixture thereof. The dicarboxylic acid can be glutaric acid, adipic acid, azelaic acid, malonic acid, suberic acid, sebacic acid, succinic acid, oxalic acid, pimelic acid, derivatives thereof, or any mixture thereof. The epihalohydrin can be epichlorohydrin, epibromohydrin, epifluorohydrin, epiiodohydrin, or any mixture thereof.

Illustrative unsaturated glycidyl ethers can be represented by general Formula VII discussed and described above. Suitable reaction products produced by reacting one or more polyamidoamines and one or more unsaturated glycidyl ethers and methods for making the reaction products can be as discussed and described in U.S. Pat. Nos. 2,864,775 and 3,280,054.

The product(s) formed by reacting the polyamidoamine(s) and the unsaturated glycidyl ether(s) can act or serve as active reducers. As used herein, the term “active reducer” refers to compounds that can participate in a cross-linking reaction, e.g., have double bonds, and also have one or more groups that can be oxidized, e.g., a tertiary amine.

In one or more embodiments, the unsaturated prepolymer can be combined with water to produce a water and unsaturated prepolymer mixture. For example, water can be mixed, blended, or otherwise combined with the unsaturated prepolymer to produce the water and unsaturated prepolymer mixture. The unsaturated prepolymer can be soluble in water. The unsaturated prepolymer can be dissolved in water to produce an aqueous unsaturated prepolymer solution. The unsaturated prepolymer can be combined with water to form an aqueous suspension, emulsion, or dispersion. The amount of the water, combined with the unsaturated prepolymer can be of about 1 wt %, about 5 wt %, about 10 wt %, about 15 wt %, about 20 wt %, about 25 wt %, about 30 wt %, or about 35 wt % to about 50 wt %, about 55 wt %, about 60 wt, about 65 wt %, about 70 wt %, or about 75 wt %, based on the combined weight of the water and the unsaturated prepolymer. The unsaturated polyester prepolymer combined with water can have a viscosity of about 20 cP, about 100 cP, 1,000 cP, about 5,000 cP, or about 10,000 cP to about 50,000 cP, about 100,000 cP, about 200,000 cP, or about 300,000 cP at a temperature of about 25° C.

As used herein, the solids concentration or solids content of a compound combined with one or more liquid mediums, e.g., the polyphenolic compound and/or the unsaturated compound, as understood by those skilled in the art, can be measured by determining the weight loss upon heating a small sample, e.g., 1-5 grams of the compound, to a suitable temperature, e.g., 125° C., and a time sufficient to remove any liquid combined therewith. By measuring the weight of the sample before and after heating, the percent solids in the sample can be directly calculated or otherwise estimated.

In one or more embodiments, one or more catalysts or unsaturated polyurethane prepolymer catalysts can be used to accelerate the rate of reaction of the polyisocyanate and the polyol to produce the unsaturated polyurethane prepolymer. Suitable catalysts can include, but are not limited to, dibutyl tin dilaurate. In one or more embodiments, one or more inhibitors can be used to slow the cross-linking reaction. Suitable inhibitors can include, but are not limited to, benzoyl chloride and monophenyldichlorophosphate.

In one or more embodiments, the unsaturated prepolymer, can have a pH of about 0.5, about 2, about 3, or about 4 to about 7, about 7.5, about 8, about 8.5, or about 9. For example, the unsaturated polyester prepolymer can have a pH of about 1.5 to about 9, about 2.5 to about 7, about 1 to about 5, about 5 to about 8, or about 3 to about 6.

Any suitable free radical precursor or combination of free radical precursors can be used to produce the binder composition. The free radical precursor can be a solid, liquid, gas, or multi-phase. As used herein, the phrase “free radical precursor” refers to any compound or mixture of compounds that can generate radicals when subjected to predetermined conditions. For example, the free radical precursor can be a compound or mixture of compounds that can generate radicals when heated to a predetermined temperature. For example, if the free radical precursor includes an oxidant, e.g., an inorganic oxidant such as hydrogen peroxide, and a catalyst or free radical precursor catalyst, e.g., a transition metal catalyst, the free radical precursor can generate radicals when the oxidant is subjected to reaction with the catalyst. As such, in one or more embodiments, the free radical precursor can include one or more oxidants and one or more catalysts.

Illustrative free radical precursors can include, but are not limited to inorganic and/or organic peroxy compounds, ozonides, halogen containing oxidants, or any combination thereof. Illustrative inorganic peroxy compounds can include, but are not limited to, hydrogen peroxide, hydrogen peroxide generating compounds, e.g., alkali metal salts of percarbonate, perborate, peroxysulfate, peroxyphosphate, and/or peroxysilicate, and/or corresponding weak acids. Illustrative organic peroxy compounds can include, but are not limited to t-butyl peroxide, benzoyl peroxide, peroxy carboxylic acids, e.g., peracetic acid and/or perbenzoic acid, hydroperoxides, e.g. t-butyl hydroperoxide. Illustrative halogen containing oxidants can include, but are not limited to, alkali metal chlorite, alkali metal hypochlorite, chlorine dioxide, and/or a chloro sodium salt of cyanuric acid. An illustrative ozonide can include, but is not limited to, dimethyloxirane. An illustrative azo compound can include, but is not limited to azobisisobutyronitrile (AIBN). In one or more embodiments, the free radical precursor can be or include one or more inorganic oxidants. In one or more embodiments, the free radical precursor can be or include one or more inorganic peroxy compounds. In one or more embodiments, the free radical precursor can be or include hydrogen peroxide.

If the free radical precursor includes one or more oxidants, the one or more oxidants can be present in an amount of about 1 wt %, about 3 wt %, about 5 wt %, about 7 wt %, about 9 wt %, about 10 wt %, about 12 wt %, about 15 wt %, about 20 wt %, about 25 wt %, about 30 wt %, about 35 wt %, or about 40 wt % to about 60 wt %, about 65 wt %, about 70 wt %, about 75 wt %, about 80 wt %, about 85 wt %, about 90 wt %, about 95 wt %, or about 99 wt %, based on the combined weight of the polyphenolic compound, the unsaturated compound, and the free radical precursor. For example, the amount of the free radical precursor in the binder composition can be about 7 wt % to about 99 wt %, about 10 wt % to about 80 wt %, about 15 wt % to about 70 wt %, about 17 wt % to about 66 wt %, about 10 wt % to about 45 wt %, about 35 wt % to about 75 wt %, about 15 wt % to about 25 wt %, about 20 wt % to about 35 wt %, about 30 wt % to about 50 wt %, about 35 wt % to about 60 wt %, or about 45 wt % to about 80 wt %, based on the combined weight of the polyphenolic compound, the unsaturated compound, and the free radical precursor. In another example, the amount of the free radical precursor in the binder composition can be present in an amount of at least 3 wt %, at least 5 wt %, at least 6 wt %, at least 7 wt %, at least 8 wt %, at least 9 wt %, at least 10 wt %, at least 15 wt %, at least 20 wt %, at least 25 wt % at least 20 wt %, at least 35 wt %, at least 40 wt %, or at least 45 wt % to about 50 wt %, about 55 wt %, about 60 wt %, about 65 wt %, about 70 wt %, about 75 wt %, about 80 wt %, about 85 wt %, about 90 wt %, or about 95 wt, based on the combined weight of the polyphenolic compound, the unsaturated compound, and the free radical precursor. In another example, the amount of the free radical precursor in the binder composition can be less than 95 wt %, less than 90 wt %, less than 85 wt %, less than 80 wt %, less than 75 wt %, less than 70 wt %, less than 60 wt %, less than 55 wt %, less than 50 wt %, less than 45 wt %, or less 40 wt % and greater than 2 wt %, greater than 5 wt %, greater than 6 wt %, greater than 7 wt %, greater than 8 wt %, greater than 9 wt %, greater than 10 wt %, greater than 15 wt %, greater than 20 wt %, or greater than 25 wt %, based on the combined weight of the polyphenolic compound, the unsaturated compound, and the free radical precursor.

The free radical precursor can be combined with one or more liquid mediums. For example, the free radical precursor can be or include an aqueous solution of hydrogen peroxide. The concentration of free radical precursor, e.g., hydrogen peroxide combined with a liquid medium such as water, can be of about 1 wt %, about 3 wt %, about 5 wt %, about 10 wt %, about 15 wt %, about 20 wt %, about 25 wt %, or about 30 wt % to about 50 wt %, about 60 wt %, about 70 wt %, about 80 wt %, about 90 wt %, or about 98 wt %, based on the combined weight of the free radical precursor and the liquid medium.

The catalyst that can be present as a component of the free radical precursor or as the free radical precursor can also be referred to as an initiator, a promoter, a reducer, and/or an accelerator. Suitable catalysts can be or include, but are not limited to, metal ions, tertiary amines, polymeric tertiary amines, phosphates, bisulfites, metabisulfites, tetraacetylethylenediamine, cyanamides, ultraviolet light, or any combination thereof. In one or more embodiments, in addition to or in lieu of contacting the lignocellulose substrates (discussed below) with a free radical precursor and/or catalyst, ultrasonic waves, photo-Fenton and/or electro-Fenton reactions (in situ generation of hydroxyl radicals by radiation or electric currents) can be used. In one or more embodiments, the catalyst can be or include one or more transition metals with coordinated Lewis bases.

Illustrative metal ions can include, but are not limited to, metal ions of iron, copper, manganese, tungsten, molybdenum, or any combination or mixture thereof. The metal can be in the form of an oxide. The metal can be in the form of a salt or complex, e.g., bound to one or more complexing agents or compounds. Illustrative ions or complexing compounds can include, but are not limited to, cyanide (CN⁻), sulfate (SO₄ ²⁻), ethylenediaminetetraacetic acid (EDTA), ethylenediamine-N,N′-disuccinic acid (EDDS), ethyleneglycol bis(2-aminoethylether)-N,N,N′,N′-tetraacetic acid (EGTA), diethylenetriaminepentaacetic acid (DTPA), trans-1,2-diaminocyclohexane tetraacetic acid (CDTA), iminodisuccinate (IDS), nitrilotriacetic acid (NTA), or any mixture thereof. Other complexing compounds can include phosphates, or complexing agents based on phosphonic acid, oxalic acid, ascorbic acid, nitriloacetate, gallic acid, fulvic acid, or polyoxometalates.

The metal ions can include compounds or complexes containing iron ions (e.g., Fe²⁺ or Fe³⁺), such as iron(II) sulfate, iron(II) oxide, iron(III) sulfate, iron(III) oxide. Other iron ion containing catalyst can include, but are not limited to, ferricyanide ([Fe(CN)₆]³⁻), ferrocyanide ([Fe(CN)₆]⁴⁻), and/or nitroprusside ([Fe(CN)₅NO]²⁻). For example, the catalyst can be or include, but is not limited to, potassium ferricyanide (K₃[Fe(CN)₆]), potassium ferrocyanide (K₄[Fe(CN)₆]), ammonium ferricyanide hydrate ((NH₄)₃[Fe(CN)₆].xH₂O), ammonium ferrocyanide hydrate ((NH₄)₄[Fe(CN)₆].xH₂O), sodium ferricyanide decahydrate (Na₃[Fe(CN)₆].10H₂O), sodium ferrocyanide decahydrate (Na₄[Fe(CN)₆].10H₂O), sodium nitroprusside dihydrate (Na₂[Fe(CN)₅NO].2H₂O). Other suitable catalyst that contain iron can include, but are not limited to, Fe[EDTA], Fe[EDDS], Fe[DTPA], Fe[EGTA], Fe[CDTA], Fe[IDS], or any mixture thereof. In some embodiments, the catalyst can include ferricyanide, e.g., potassium ferricyanide, a complex of iron (e.g., ferric and/or ferrous) and ethylenediaminetetraacetic acid (EDTA), a complex of iron (e.g., ferric and/or ferrous) and (S,S)-ethylenediamine-N,N′-disuccinic acid ((S,S)-EDDS), a complex of iron (e.g., ferric and/or ferrous) and (R,R)-ethylenediamine-N,N′-disuccinic acid ((R,R)-EDDS), a complex of iron (e.g., ferric and/or ferrous) and (R,S)-ethylenediamine-N,N′-disuccinic acid ((R,S)-EDDS), a complex of iron (e.g., ferric and/or ferrous) and diethylenetriaminepentaacetic acid (DTPA), a complex of iron (e.g., ferric and/or ferrous) and trans-1,2-diaminocyclohexane tetraacetic acid (CDTA), a complex of iron (e.g., ferric and/or ferrous) and iminodisuccinate (IDS), hydrates thereof, or any mixture thereof.

Tertiary amines can be represented by the general formula NR¹⁴R¹⁵R¹⁶, where each R¹⁴, R¹⁵, and R¹⁶ can independently be an alkyl, a cycloalkyl, a heterocycloalkyl, an aryl, a heteroaryl, or a substituted aryl. The alkyl can include branched or unbranched alkyls having 1 carbon atom to about 15 carbon atoms, or 1 carbon atom to about 8 carbon atoms. Illustrative alkyls can include, but are not limited to, methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, t-butyl, n-pentyl, n-hexyl, and ethylhexyl, isomers thereof, or any mixture thereof. The cycloalkyls can include 3 carbon atoms to about 7 carbon atoms. Illustrative cycloalkyls can include, but are not limited to, cyclopentyl, substituted cyclopentyl, cyclohexyl, and substituted cyclohexyl. The term “aryl” refers to an aromatic substituent containing a single aromatic ring or multiple aromatic rings that are fused together, linked covalently, or linked to a common group such as a methylene or ethylene moiety. More specific aryl groups can include one aromatic ring or two or three fused or linked aromatic rings, e.g., phenyl, naphthyl, biphenyl, anthracenyl, phenanthrenyl, and the like. The aryl substituents can include 1 carbon atom to about 20 carbon atoms. The term “heteroatom-containing,” as in a “heteroatom-containing cycloalkyl group,” refers to a molecule or molecular fragment in which one or more carbon atoms is replaced with an atom other than carbon, e.g., nitrogen, oxygen, sulfur, phosphorus, boron, or silicon. Similarly, the term “heteroaryl” refers to an aryl substituent that is heteroatom-containing. The term “substituted,” as in “substituted aryls,” refers to a molecule or molecular fragment in which at least one hydrogen atom bound to a carbon atom is replaced with one or more substituents that are functional groups such as hydroxyl, alkoxy, alkylthio, phosphino, amino, halo, silyl, and the like. Illustrative tertiary amines can include, but are not limited to, trimethylamine, triethylamine, triethanolamine, or any combination thereof. Illustrative polymeric tertiary amines can include, but are not limited to, poly(N-methyldiallyl amine), poly(N-dimethylvinyl amine), copolymers of N-dimethylvinyl amine, or any combination thereof.

Illustrative phosphates can be or include, but are not limited to, potassium phosphate, sodium phosphate, ammonium phosphate, or any combination or mixture thereof. Illustrative bisulfites can include sodium bisulfate. Illustrative metabisulfites can be or include, but are not limited to, sodium metabisulfite, potassium metabisulfite, or any combination or mixture thereof. Illustrative cyanamides can include, but are not limited to, cyanamide, calcium cyanamide, sodium hydrogen cyanamide, or any combination thereof.

The catalyst, if combined with a liquid medium, can have a total concentration of solids of about 0.001 wt % to about 99.9 wt %. In some examples, if the catalyst is combined with a liquid medium, the catalyst and liquid medium mixture can have a concentration of solids of about 0.1 wt %, about 0.5 wt %, about 1 wt %, or about 2 wt % to about 4 wt %, about 5 wt %, about 6 wt %, about 7 wt %, or about 8 wt %, based on the combined weight of the catalyst and the liquid medium.

The amount of catalyst present in the binder composition can widely vary. For example, the amount of catalyst in the binder composition can be about 0.01 wt %, about 0.1 wt %, about 0.5 wt %, about 1 wt %, or about 3 wt % to about 8 wt %, about 10 wt %, about 12 wt %, about 14 wt %, about 17 wt %, or about 20 wt %, based on the combined weight of the polyphenolic compound, the unsaturated compound, and the free radical precursor, where the catalyst is a component or part of the free radical precursor. In another example, the amount of catalyst in the binder composition can be about 1 wt % to about 5 wt %, about 3 wt % to about 13 wt %, about 0.1 wt % to about 9 wt %, about 1 wt % to about 7 wt %, about 7 wt % to about 15 wt %, or about 0.2 wt % to about 15 wt %, based on the combined weight of the polyphenolic compound, the unsaturated compound, and the free radical precursor, where the catalyst is a component or part of the free radical precursor. In another example, the amount of catalyst in the binder composition can be about 0.0001 wt %, about 0.001 wt %, about 0.01 wt %, about 0.1 wt %, about 0.13 wt %, or about 0.15 wt % to about 0.17 wt %, about 0.2 wt %, about 0.23 wt %, about 0.25 wt %, about 0.27 wt %, about 0.3 wt %, about 0.35 wt %, about 0.4 wt %, about 0.5 wt %, about 1 wt %, about 2 wt %, about 3 wt %, about 4 wt %, about 5 wt %, about 6 wt %, about 7 wt %, about 8 wt %, about 9 wt %, or about 10 wt %, based on the combined weight of the polyphenolic compound, the unsaturated compound, the catalyst, and the oxidant, where the catalyst is a component of the free radical precursor. In another example, the amount of catalyst in the binder composition can be about 0.01 wt % to about 2 wt %, about 0.17 wt % to about 0.37 wt %, about 0.19 wt % to about 0.31 wt %, about 0.2 wt % to about 0.29 wt %, about 0.05 wt % to about 1.5 wt %, or about 0.2 wt % to about 2 wt %, based on the combined weight of the polyphenolic compound, the unsaturated compound, the catalyst, and the oxidant, where the catalyst is a component of the free radical precursor.

In one or more embodiments, any one or more of the polyphenolic compound, the unsaturated compound, and the free radical precursor can be combined with a liquid medium. The polyphenolic compound, the unsaturated compound, and the free radical precursor, when combined with the liquid medium, can have a total concentration of solids of about 1 wt % to about 99 wt %. For example, the polyphenolic compound and/or the unsaturated compound combined with a liquid medium can have a concentration of solids of about 5 wt %, about 10 wt %, about 15 wt %, or about 20 wt % to about 40 wt %, about 50 wt %, about 60 wt %, about 70 wt %, or about 80 wt %, based on the combined weight of the polyphenolic compound and/or the unsaturated compound and the liquid medium. In another example, the polyphenolic compound and/or the unsaturated compound combined with a liquid medium can have a concentration of solids of about 40% to about 60%, about 45% to about 55%, or about 47% to about 50%, based on the combined weight of the polyphenolic compound and/or the unsaturated compound and the liquid medium. In another example, the polyphenolic compound and/or the unsaturated compound combined with a liquid medium can have a concentration of solids of about 10% to about 30%, about 15% to about 35%, about 20% to about 40%, about 25% to about 45%, about 20% to about 50%, or about 35% to about 55%, based on the combined weight of the polyphenolic compound and/or the unsaturated compound and the liquid medium.

As noted above, the binder composition can be mixed, blended, stirred, contacted, or otherwise combined with one or more lignocellulose substrates to produce a mixture. Combining the free radical precursor with at least one unsaturated compound and at least one polyphenolic compound, a binder composition having desired properties can exhibit improved properties attributable to each of the unsaturated compound and the polyphenolic compound when each used with the same free radical precursor alone. For example, the unsaturated compound, when combined with the free radical precursor in the absence of the polyphenolic compound, can be used to make composite products, e.g., composite lignocellulose products, that have outstanding internal bond strength, but a low resistance to water absorption. Additionally, a binder composition that includes only the unsaturated compound and the free radical precursor exhibits little, if any, tack. In contrast, a binder composition that includes only the polyphenolic compound and the free radical precursor can be used to make composite products, e.g., composite lignocellulose products, that have good internal bond strength (not as high as the unsaturated compound and good resistance to water absorption. The binder that includes only the polyphenolic compound and the free radical precursor also exhibits good tack as compared to the binder composition that includes only the unsaturated compound and the free radical precursor. Accordingly, combing both the unsaturated compound and the polyphenolic compound in the presence of the free radical precursor can provide a desired balance of properties of the binder composition, e.g., desired tack, and/or desired composite product properties, e.g., internal bond strength and/or resistance to water absorption.

In one or more embodiments, the components of the binder composition can be combined with the lignocellulose substrates in any order or combination with respect to one another such that the binder composition is formed in the presence of the one or more lignocellulose substrates. For example, the unsaturated compound and the polyphenolic compound can be combined with one another to produce a partial or intermediate binder composition, the partial composition can be combined with the lignocellulose substrates, to produce a partial mixture, and the free radical precursor can be combined with the partial mixture to produce the mixture or the resinated furnish. In another example, the components of the binder composition can independently be combined with the lignocellulose substrates in any order or sequence to produce the mixture or the resinated furnish.

If the free radical precursor includes two or more components, e.g., a catalyst and an oxidant, the components of the free radical precursor can be combined with the lignocellulose substrates and the optional compound having at least two hydrogen atoms that are abstractable in the presence of hydroxyl radicals in any order or sequence. For example, if the free radical precursor includes a catalyst and an oxidant, the catalyst can be combined with the lignocellulose substrates to produce a first partial mixture and the oxidant can be combined with the first partial mixture to produce the mixture or vice versa. In another example, the catalyst and the compound having at least two hydrogen atoms that are abstractable in the presence of hydroxyl radicals can be combined with one another to produce a first partial mixture, the first partial mixture can be combined with the lignocellulose substrates to produce a second partial mixture, and the oxidant can be combined with the second partial mixture to produce the mixture. In other examples, the oxidant and the compound having at least two hydrogen atoms that are abstractable in the presence of hydroxyl radicals can be combined with one another to produce a first partial mixture, the first partial mixture can be combined with the lignocellulose substrates to produce a second partial mixture, and the catalyst can be combined with the second partial mixture to produce the mixture. In another example, the oxidant and the catalyst can be combined with one another to produce a first partial mixture, the first partial mixture can be combined with the lignocellulose substrates to produce a second partial mixture, and the compound having at least two hydrogen atoms that are abstractable in the presence of hydroxyl radicals can be combined with the second partial mixture to produce the mixture.

The components of the resinated furnish can be introduced or otherwise contacted with one another via any suitable delivery method. For example, the lignocellulose substrates can be in a vessel or other container and the binder composition or one or more components of the binder composition can be sprayed or otherwise directed onto the lignocellulose substrates to produce the resinated furnish. In another example, the binder composition or one or more components of the binder composition can be poured or brushed onto the lignocellulose substrates. In another example, the lignocellulose substrates can be directed, transported, introduced, or otherwise conveyed into a vessel already containing any one or more of the other components of the mixture. Said another way, the lignocellulose substrates can be dipped, soaked, or otherwise contacted with the binder composition or one or more components of the binder composition. In another example, the components of the binder composition can be added or combined with the lignocellulose substrates separately or independently from one another in any order or sequence. In another example, two or more components of the binder composition can be combined with one another to form a partial binder composition, e.g., the polyphenolic compound, the unsaturated compound, and a catalyst component of the free radical precursor, and the partial binder composition can be combined with the lignocellulose substrates to produce a partial resinated mixture. The remaining component, e.g., an oxidant, can be combined with the partial resinated mixture or the partial resinated furnish to produce the resinated furnish.

The amount of the polyphenolic compound in the resinated furnish can be of about 0.5 wt %, about 1 wt %, about 3 wt %, about 5 wt %, about 7 wt %, about 10 wt %, about 12 wt %, or about 15 wt % to about 20 wt %, about 23 wt %, about 25 wt %, about 27 wt %, about 30 wt % about 33 wt %, or about 35 wt %, based on the dry weight of the lignocellulose substrates. For example, the amount of the polyphenolic compound in the resinated furnish can be about 1 wt % to about 6 wt %, about 2 wt % to about 10 wt %, about 4 wt % to about 8 wt % about 6 wt % to about 12 wt %, about 8 wt % to about 18 wt %, about 10 wt % to about 25 wt %, about 15 wt % to about 30 wt %, or about 3 wt % to about 9 wt %, based on the dry weight of the lignocellulose substrates.

The amount of the unsaturated compound in the resinated furnish can be about 00.5 wt %, about 1 wt %, about 3 wt %, about 5 wt %, about 7 wt %, about 10 wt %, about 12 wt % to about 14 wt %, about 16 wt %, about 18 wt %, about 20 wt % about 22 wt %, or about 24 wt %, based on the dry weight of the lignocellulose substrates. For example, the amount of the unsaturated compound in the resinated furnish can be about 0.5 wt % to about 3 wt %, about 1.5 wt % to about 4 wt %, about 2 wt % to about 6 wt %, about 3 wt % to about 5 wt %, about 6 wt % to about 10 wt %, about 3 wt % to about 15 wt %, or about 7 wt % to about 19 wt %, based on the dry weight of the lignocellulose substrates.

The amount of the free radical precursor in the resinated furnish can be about 0.1 wt %, about 0.5 wt %, about 1 wt %, about 2 wt %, about 3 wt %, about 4 wt %, about 5 wt %, about 7 wt %, or about 10 wt % to about 15 wt %, about 17 wt %, about 19 wt %, about 21 wt %, about 23 wt %, about 25 wt %, about 27 wt %, or about 29 wt %, based on the dry weight of the lignocellulose substrates. For example, the amount of the free radical precursor in the resinated furnish can be about 0.1 wt % to about 8 wt %, about 0.5 wt % to about 6 wt %, about 1 wt % to about 5 wt %, about 2 wt % to about 4 wt %, about 4 wt % to about 12 wt %, about 6 wt % to about 16 wt %, about 10 wt % to about 22 wt %, or about 3 wt % to about 21 wt %, based on the dry weight of the lignocellulose substrates.

The amount of the oxidant in the resinated furnish can be about 0.1 wt %, about 0.5 wt %, about 1 wt %, about 2 wt %, about 3 wt %, about 4 wt %, about 5 wt %, or about 7 wt % to about 9 wt %, about 11 wt %, about 13 wt %, about 15 wt %, about 17 wt %, or about 19 wt %, based on the dry weight of the lignocellulose substrates. For example, the amount of the oxidant in the resinated furnish can be about 0.1 wt % to about 3 wt %, about 1 wt % to about 5 wt %, about 2 wt % to about 6 wt %, about 2.5 wt % to about 10 wt %, about 3 wt % to about 6 wt %, about 4 wt % to about 14 wt %, about 6 wt % to about 18 wt %, about 1 wt % to about 11 wt %, or about 2.5 wt % to about 5.5 wt %, based on the dry weight of the lignocellulose substrates.

The amount of the catalyst in the resinated furnish can be about 0.001 wt %, about 0.005 wt %, about 0.01 wt %, about 0.03 wt %, about 0.05 wt %, about 0.07 wt %, about 0.1 wt %, about 0.12 wt %, about 0.14 wt %, about 0.16 wt %, or about 0.18 wt % to about 0.4 wt %, about 0.8 wt %, about 1 wt %, about 1.5 wt %, about 2 wt %, about 2.5 wt %, about 3 wt %, about 3.5 wt %, about 4 wt %, about 4.5 wt %, or about 5 wt %, based on the dry weight of the lignocellulose substrates. For example, the amount of the catalyst in the resinated furnish can be about 0.05 wt % to about 0.5 wt %, about 0.1 wt % to about 0.4 wt %, about 0.15 wt % to about 0.35 wt %, about 0.2 wt % to about 0.45 wt %, about 0.3 wt % to about 2 wt %, about 0.15 wt % to about 4 wt %, about 1 wt % to about 3 wt %, about 0.2 wt %% to about 4.5 wt %, or about 0.1 wt % or about 0.25 wt %, based on the dry weight of the lignocellulose substrates.

The resinated furnish can be heated to produce a lignocellulose containing composite product or “composite product.” For example, the mixture can be heated to a temperature of about 60° C., about 90° C., about 120° C., about 150° C., or about 160° C. to about 170° C., about 200° C., about 230° C., about 260° C., or about 300° C. to produce the composite product. In another example, the mixture can be heated to a temperature of at least 60° C., at least 70° C., at least 80° C., at least 90° C., at least 100° C., at least 110° C., at least 120° C., at least 130° C., or at least 140° C. to about 150° C., about 155° C., about 160° C., about 165° C., about 170° C., about 180° C., about 200° C., about 225° C., about 250° C., about 275° C., or about 300° C. In another example, the mixture can be heated to a temperature of about 140° C. to about 200° C., about 155° C. to about 175° C., about 160° C. to about 210° C., about 160° C. to about 175° C., or about 145° C. to about 225° C.

In one or more embodiments, the resinated furnish can be heated in air. In one or more embodiments, the mixture can be heated in an inert atmosphere or substantially an inert atmosphere such as nitrogen. If the mixture is heated in a substantially inert atmosphere the amount of oxygen can be less than 5 mol %, less than 3 mol %, less than 1 mol %, less than 0.5 mol %, or less than 0.1 mol % oxygen. Suitable inert gases can include, but are not limited to, nitrogen, argon, or a mixture thereof.

Heating the binder composition and/or the resinated furnish can cause or promote the at least partial curing of the binder composition to produce the composite product. As used herein, the terms “curing,” “cured,” “at least partially curing,” “at least partially cured,” and similar terms are intended to refer to the structural and/or morphological change that occurs in the mixture, such as by covalent chemical reaction (crosslinking), ionic interaction or clustering, phase transformation or inversion, and/or hydrogen bonding when the is subjected to conditions sufficient, e.g., sufficiently heated, to cause the properties of a flexible, porous substrate, such as a nonwoven mat or blanket of lignocellulose substrates and/or a rigid or semi-rigid substrate, such as a wood or other lignocellulose containing board or sheet, to which an effective amount of the binder composition has been applied, to be altered.

When the binder composition is heated, the resinated furnish can contain at least a portion of the free radical precursor initially added to and present in the binder composition. Said another way, at least a portion of the free radical precursor can remain unreacted or otherwise in the same form as when combined with the additional components of the binder composition, at least until the resinated furnish is heated. For example, if the free radical precursor includes one or more oxidants, e.g., hydrogen peroxide (H₂O₂), at least a portion of the oxidant in the form of hydrogen peroxide can be present when heating of the mixture is initiated or started. In one or more embodiments, the resinated furnish can contain at least 1 wt %, at least 3 wt %, at least 5 wt %, at least 7 wt %, at least 9 wt %, 11%, at least 13%, at least 15%, at least 20%, at least 25%, at least 30%, at least 35%, at least 40%, at least 45%, at least 50%, at least 55%, at least 60%, at least 65%, or at least 70% of the total amount of free radical precursor initially present in the resinated furnish, i.e., the total amount of the free radical precursor combined with the plurality of lignocellulose substrates, the polyphenolic compound, and the unsaturated compound, when the resinated furnish is heated. In another example, the resinated furnish can contain about 11% to about 95%, about 15% to about 85%, about 20% to about 90%, about 30% to about 80%, about 11% to about 100%, about 35% to about 75%, about 40% to about 70%, about 50% to about 70%, about 60% to about 80%, about 65% to about 85%, or about 30% to about 95% of the total amount of free radical precursor initially present in the resinated furnish when the resinated furnish is heated. In one or more examples, if the resinated furnish includes about 5 wt % free radical precursor, based on the dry weight of the lignocellulose substrates when the mixture is initially formed, when the mixture is heated to a temperature of about 60° C. or more at least 11% of the free radical precursor can be present in the resinated furnish. Said another way, if the resinated furnish contains about 5 wt % of the one or more free radical precursors, based on the dry weight of the lignocellulose substrates, upon preparation or formation of the resinated furnish, when heating the resinated furnish is initiated or started, the resinated furnish can have a free radical precursor concentration of at least 11% of the initial 5 wt % or 0.55 wt %, based on the dry weight of the lignocellulose substrates.

In one or more embodiments, the amount of the metal, if present in a catalyst that includes the metal bound to complexing agent, that can remain bound to the complexing agent until the mixture is heated, e.g., to a temperature of about 60° C. to about 300° C., can be at least 1 wt %, at least 3 wt %, at least 5 wt %, at least 7 wt %, at least 9 wt %, at least 11%, at least 13%, at least 15%, at least 20%, at least 25%, at least 30%, at least 35%, at least 40%, at least 45%, at least 50%, at least 55%, at least 60%, at least 65%, or at least 70% of the amount of metal that was initially present in the mixture and bound to the complexing agent. In another example, the amount of the metal, if present in the catalyst, that can remain bound to the complexing agent until the mixture is heated, e.g., to a temperature of about 60° C. to about 300° C., can be about 11% to about 95%, about 15% to about 85%, about 20% to about 90%, about 30% to about 80%, about 11% to about 100%, about 35% to about 75%, about 40% to about 70%, or about 30% to about 95% of the amount of the metal initially present in the mixture and bound to the complexing agent.

In one or more embodiments, the amount of the one or more free radical precursors present when the resinated furnish is heated, e.g., to a temperature of about 60° C. to about 300° C., can be at least 0.5 wt %, at least 0.7 wt %, at least 1 wt %, at least 1.2 wt %, at least 1.5 wt %, at least 1.7 wt %, at least 2 wt %, at least 2.2 wt %, at least 2.5 wt %, at least 2.7 wt %, at least 3 wt %, at least 3.2 wt %, at least 3.5 wt %, at least 3.7 wt %, at least 4 wt %, at least 4.2 wt %, at least 4.5 wt %, at least 4.7 wt %, or at least 5 wt %, based on the dry weight of the plurality of lignocellulose substrates. For example, the amount of the one or more free radical precursors present when the resinated furnish is heated can be about 1 wt %, about 1.5 wt %, about 1.6 wt %, about 1.8 wt %, or about 2.1 wt % to high of about 5 wt %, about 7 wt %, about 10 wt %, about 15 wt %, about 20 wt % or greater, based on the dry weight of the plurality of lignocellulose substrates. In another example, the amount of the one or more free radical precursors present when the resinated furnish is heated can be about 1 wt % to about 10 wt %, about 1.5 wt % to about 7 wt %, about 2 wt % to about 6 wt %, about 2.5 wt % to about 8 wt %, about 3 wt % to about 5.5 wt %, about 4 wt % to about 6.5 wt %, about 2.2 wt % to about 11 wt %, or about 2.3 wt % to about 6.3 wt %, based on the dry weight of the plurality of lignocellulose substrates.

The pH of the resinated furnish can be acidic, neutral, or basic. For example, the pH of the resinated furnish can be about 1, about 2, or about 3 to about 4, about 5, about 6, about 7, or about 8. In another example, the pH of the resinated furnish can be about 1 to about 6, about 1.5 to about 5.5, about 2.5 to about 4.5, about 2 to about 3.5, or about 2.5 to about 3.5. The pH of the resinated furnish can be adjusted to any desired pH by combining one or more base compounds, one or more acid compounds, or a combination of one or more base compounds and one or more acid compounds therewith.

Illustrative base compounds that can be used to adjust the pH of the resinated furnish can include, but are not limited to, hydroxides, carbonates, ammonia, amines, or any combination thereof. Illustrative hydroxides can include, but are not limited to, sodium hydroxide, potassium hydroxide, ammonium hydroxide (e.g., aqueous ammonia), lithium hydroxide, and cesium hydroxide. Illustrative carbonates can include, but are not limited to, sodium carbonate, sodium bicarbonate, potassium carbonate, and ammonium carbonate. Illustrative amines can include, but are not limited to, trimethylamine, triethylamine, triethanolamine, diisopropylethylamine (Hunig's base), pyridine, 4-dimethylaminopyridine (DMAP), and 1,4-diazabicyclo[2.2.2]octane (DABCO).

Illustrative acid compounds that can be used to adjust the pH of the resinated furnish can include, but are not limited to, one or more mineral acids, one or more organic acids, one or more acid salts, or any combination thereof. Illustrative mineral acids can include, but are not limited to, hydrochloric acid, nitric acid, phosphoric acid, sulfuric acid, or any combination thereof. Illustrative organic acids can include, but are not limited to, acetic acid, formic acid, citric acid, oxalic acid, uric acid, lactic acid, or any combination thereof. Illustrative acid salts can include, but are not limited to, ammonium sulfate, sodium bisulfate, sodium metabisulfite, or any combination thereof.

The resinated furnish can include one or more liquid mediums. The one or more liquid mediums can be present in any one or more of the lignocellulose substrates, the free radical precursor, the polyphenolic compound, and/or the unsaturated compound. The liquid medium can be or include, but is not limited to, water, alcohols, glycols, acetonitrile, dimethyl sulfoxide, N,N-dimethylformamide, N-methylpyrrolidone, or any combination thereof. Suitable alcohols can include, but are not limited to, methanol, ethanol, propanol, isopropanol, butanol, or any combination thereof. Suitable glycols can include, but are not limited to, ethylene glycol, propylene glycol, or a combination thereof. As used herein, the terms “aqueous medium” and “aqueous liquid” can be or include water and/or mixtures composed of water and/or other water-miscible solvents. Illustrative water-miscible solvents can include, but are not limited to, alcohols, ethers, amines, other polar aprotic solvents, and the like. In at least one example, the liquid medium can be water and the catalyst, the oxidant, the polyphenolic compound, and/or the unsaturated compound can be combined with water.

The resinated furnish can have a liquid, e.g., water, content of about 1 wt %, about 3 wt %, about 5 wt %, or about 10 wt % to high of about 12 wt %, about 14 wt %, about 16 wt %, about 18 wt %, about 20 wt %, about 22 wt %, or about 24 wt %. For example, when the resinated furnish contains water as the liquid, the resinated furnish can have a moisture content of about 10 wt % to about 25 wt %, about 12 wt % to about 20 wt %, about 11 wt % to about 19 wt %, about 13 wt % to about 18 wt %, about 15 wt % to about 18 wt %, about 12 wt % to about 17 wt %, or about 14 wt % to about 17 wt %, based on the total weight of the resinated furnish.

The lignocellulose substrates can include any one or more of the plant and vegetable materials discussed and described above with reference to the source for the lignins and tannins. As used herein, the term “lignocellulose” refers to a material that includes lignin, cellulose, hemicellulose, or any combination thereof. The starting material, from which the lignocellulose substrates can be or can be derived from, can be shaped, reduced, or otherwise formed to the appropriate dimensions by various processes such as hogging, grinding, milling, tearing, shredding, and/or flaking. Other processes for producing the substrates can include skiving, cutting, slicing, and/or sawing. Suitable forms of the lignocellulose substrates can be or include, but are not limited to, chips, flakes, wafers, fibers, powder, particles, shavings, sawdust or dust, veneer, strands, or any mixture thereof. Accordingly, the term “substrate” when used in conjunction with “lignocellulose” refers to lignocellulose material or lignocellulose containing material having any desired shape such as chips, flakes, wafers, fibers, powder, particles, shavings, sawdust or dust, veneer, strands, or any mixture thereof. Other suitable lignocellulose substrates can include, but are not limited to, wood chips, wood fibers, wood flakes, wood strands, wood wafers, wood shavings, wood particles, wood veneer, or any mixture thereof.

The particular configuration of the substrates can be based, at least in part, on the desired product. For example, particulates such as chips, fibers, shavings, strands, sawdust, or the like can be used for producing particleboards, fiberboards, oriented strand boards, and the like. The substrates can have a length of about 0.05 mm, about 0.1 mm, about 0.2 mm to about 1 mm, about 5 mm, about 10 mm, about 20 mm, about 30 mm, about 40 mm, about 50 mm, or about 100 mm. In another example, veneers, e.g., layers or sheets of wood, can be used for producing plywood, laminated veneer lumber, and the like. The veneers can have a thickness of about 0.8 mm, about 0.9 mm, about 1 mm, about 1.1 mm or about 1.2 mm to about 3 mm, about 4 mm, about 5 mm, about 6 mm, about 7 mm, about 8 mm, about 9 mm, or about 10 mm.

The lignocellulose substrates can include liquid on, about, and/or within the substrates. For example, the lignocellulose substrates can have a liquid, e.g., moisture, content of about 1 wt %, about 2 wt %, about 3 wt %, about 4 wt, or about 5 wt % to about 7 wt %, about 9 wt %, about 11 wt %, about 13 wt %, about 15 wt %, about 17 wt %, about 19 wt %, about 21 wt %, about 23 wt %, about 25 wt %, about 27 wt %, about 29 wt %, about 31 wt %, about 33 wt %, about 35 wt %, or about 37 wt % based on a dry weight of the lignocellulose substrate. In another example, the lignocellulose substrates can have a liquid, e.g., moisture, content of about 1 wt % to about 10 wt %, about 2 wt % to about 4 wt %, about 2 wt % to about 3 wt %, about 3 wt % to about 6 wt %, about 5 wt % to about 10 wt %, about 6 wt % to about 8 wt %, or about 4 wt % to about 9 wt %. The lignocellulose substrates can be fresh, e.g., not treated or dried, or dried and/or treated. For example, the lignocellulose substrates and/or the starting material from which the lignocellulose substrates were derived can be at least partially dried. In another example, the lignocellulose substrates can be washed and/or leached with an aqueous medium such as water.

If any one or more of the components discussed and described herein include two or more different compounds, those two or more different compounds can be present in any ratio with respect to one another. Said another way, if the mixture includes a first type and a second type of lignocellulose substrate, the free radical precursor, the polyphenolic compound, and/or the unsaturated compound, the amount of the first and second components can be present in any desired ratio. For example, if the oxidant is present in the free radical precursor and includes a first oxidant and a second oxidant, the mixture can have an oxidant composition that includes the first oxidant in an amount of about 1 wt % to about 99 wt % and conversely about 99 wt % to about 1 wt % of the second oxidant, based on the total weight of the oxidant composition, e.g., the total weight of the first and second oxidants. In another example, the amount of the first oxidant can be about 5 wt %, about 10 wt %, about 15 wt %, about 20 wt %, about 25 wt % about 30 wt %, about 35 wt %, about 40 wt %, or about 45 wt % to about 60 wt %, about 65 wt %, about 70 wt %, about 75 wt %, about 80 wt %, about 85 wt %, about 90 wt %, or about 95 wt %, based on the total weight of the first and second oxidants.

One or more salts can optionally be combined with the lignocellulose substrates, the binder composition, and/or any component of the binder composition. The amount of salt present in the resinated furnish, if present, can be about 0.1 wt %, about 1 wt %, about 2 wt %, or about 3 wt % to about 10 wt %, about 20 wt %, or about 30 wt %, based on the dry weight of the lignocellulose substrates. The one or more salts can be combined with the lignocellulose substrates, the binder composition, and/or any component of the binder composition in any order or sequence. Illustrative salts can include, but are not limited to, Al, Ca, K, Na, Cu, Zn, Mg, Mn, Ba, and/or Li cations. Suitable anions can include, but are not limited to, carbonates, chlorides, nitrates, silicates, acetates, formates, sulfates, phosphates, and/or combinations thereof.

In one or more embodiments, one or more additives can be combined with the lignocellulose substrates, binder composition, and/or any one or more components of the binder composition, to produce the resinated furnish. Illustrative additives can include, but are not limited to, waxes and/or other hydrophobic additives, water, filler material(s), extenders, surfactants, release agents, dyes, fire retardants, formaldehyde scavengers, biocides, or any combination thereof. For composite wood products, such as plywood, typical filler material(s) can include, but are not limited to, ground pecan and/or walnut shells, and typical extenders can include, for example, wheat flour. Other suitable extenders can include, but are not limited to, polysaccharides, and the like. Illustrative polysaccharides can include, but are not limited to, starch, cellulose, gums, such as guar and xanthan, alginates, pectin, gellan, or any combination thereof. Suitable polysaccharide starches can include, for example maize or corn, waxy maize, high amylose maize, potato, tapioca, and wheat starch. Other starches such as genetically engineered starches can include high amylose potato and potato amylopectin starches.

If one or more additives is present in the resinated furnish, the amount of each additive can be about 0.01 wt % to about 50 wt %, based on the total weight of the resinated furnish. For example, the amount of any given component or additive can be about 0.01 wt %, about 0.05 wt %, about 0.1 wt %, about 0.5 wt %, or about 1 wt % to about 3 wt %, about 5 wt %, about 7 wt %, or about 9 wt %, based on the total weight of the resinated furnish. In another example, the amount of any given additive or component can be about 1 wt %, about 5 wt %, about 10 wt %, about 15 wt %, or about 20 wt % to about 25 wt %, about 30 wt %, about 35 wt %, about 40 wt %, or about 45 wt %, based on the total weight of the resinated furnish. In some embodiments, one or more waxes, e.g., slack wax, can be present in the mixture and the amount of wax can about 0.1 wt %, about 0.5 wt %, or about 0.9 wt % to about 1.5 wt %, about 2 wt %, or about 3 wt %, based on the dry weight of the lignocellulose substrates.

The resinated furnish can be heated as soon as the resinated furnish is formed. The resinated furnish can be kept, held, or otherwise maintained at a temperature less than 60° C. for a period of time prior to heating the resinated furnish to a temperature of at least 60° C. At least one way an exothermic reaction between the components of the mixture can be substantially and significantly slowed and/or prevented such that the mixture does not significantly increase in temperature until the resinated furnish is intentionally heated can be to select an appropriate free radial precursor or mixture of free radical precursors. In other words, the temperature of the mixture, without external heat directed to the mixture, can remain free from or substantially free from the development of an exotherm by selecting an appropriate free radical precursor(s). The particular temperature of the resinated furnish during the time period before heating can depend, at least in part, on the ambient or environmental temperature where the resinated furnish is located. In one or more embodiments, the resinated furnish can be maintained at a temperature of less than 60° C. without any intentional removal of heat therefrom. In one or more embodiments, the resinated furnish can be maintained at a temperature of less than 60° C. with removal of heat therefrom, e.g., the mixture can be located within a refrigeration device and/or a cooled fluid such as chilled air can be directed toward and/or passed through the mixture. In one or more embodiments, the resinated furnish can be maintained at a temperature of less than 60° C. by controlling or adjusting a water concentration of the mixture. For example, increasing the water concentration of the mixture can reduce, inhibit, or prevent the resinated furnish from undergoing an exothermic reaction.

Prior to heating the resinated furnish to a temperature of at least 60° C., the mixture can be maintained at a temperature less than 60° C., less than 55° C., less than 50° C., less than 45° C., less than 40° C., less than 35° C., or less than 30° C. for at least 10 minutes, at least 13 minutes, at least 15 minutes, at least 17 minutes, at least 20 minutes, at least 23 minutes, at least 25 minutes, at least 27 minutes, at least 30 minutes, at least 33 minutes, at least 35 minutes, at least 37 minutes, at least 40 minutes, at least 43 minutes, at least 45 minutes, at least 47 minutes, at least 50 minutes, at least 53 minutes, at least 55 minutes, at least 57 minutes, or at least 60 minutes. For example, the resinated furnish can be maintained at a temperature less than 60° C. for at least 10 minutes to about 30 minutes, at least about 15 minutes to about 35 minutes, at least about 20 minutes to about 40 minutes, at least about 18 minutes to about 45 minutes, or at least about 15 minutes to about 40 minutes prior to heating the mixture to a temperature of at least 60° C. In another example, the resinated furnish can be maintained at a temperature less than 60° C. for at least 10 minutes, about 30 minutes, about 45 minutes, about 1 hour, about 2 hours, about 3 hours, about 5 hours, about 12 hours, about 18 hours, about 24 hours, or about 30 hours prior to heating the mixture to a temperature of at least 60° C.

Prior to heating the resinated furnish to a temperature of at least 60° C., the amount of energy generated from the mixture due to exothermic reaction(s) between the components of the resinated furnish can be less than 20 cal/g of the mixture, less than 18 cal/g of the mixture, less than 16 cal/g of the mixture, less than 15 cal/g of the mixture, less than 14 cal/g of the mixture, or less than 13.8 cal/g of the mixture. For example, prior to heating the resinated furnish to a temperature of at least 60° C., the amount of energy generated from the mixture due to the exothermic reaction between the components of the mixture can be less than 14 cal/g, less than 13.5 cal/g, less than 13 cal/g, less than 12.5 cal/g, less than 12 cal/g, less than 11.5 cal/g, less than 11 cal/g, less than 10.5 cal/g, less than 10 cal/g, less than 9.5 cal/g, less than 9 cal/g, less than 8.5 cal/g, less than 8 cal/g, less than 7.5 cal/g, less than 7 cal/g, less than 6.5 cal/g, less than 6 cal/g, less than 5.5 cal/g, less than 5 cal/g, less than 4.5 cal/g, less than 4 cal/g, less than 3.5 cal/g, less than 3 cal/g, less than 2.5 cal/g. less than 2 cal/g, less than 1.5 cal/g, less than 1 cal/g, or less than 0.5 cal/g of the mixture.

Illustrative composite products discussed and described herein can be or include, but are not limited to, particleboard, fiberboard, oriented strand board (“OSB”), oriented stand lumber (“OSL”), chipboard, flakeboard, waferboard, plywood such as hardwood plywood and/or softwood plywood, laminated veneer lumber (“LVL”), laminated veneer boards (“LVB”), or engineered wood flooring. Illustrative fiberboards can be or include, but are not limited to, low density fiberboard (“LDF”), medium density fiberboard (“MDF”), and/or high density fiberboard (“HDF”).

The method of making one or more composite products can include a continuous or semi-continuous blending process in which the lignocellulose substrates and the other components of the resinated furnish, e.g., the polyphenolic compound, the unsaturated compound, and the free radical precursor, can be introduced to a blender at a first or introduction region, end, area, or other location(s) configured to receive the components and the resinated furnish can be withdrawn from the blender via one or more mixture recovery outlets. The blender can be configured to contain a few hundred kilograms to several thousand kilograms. For example, in a single blender about 500 kg/hr, about 5,000 kg/hr, about 10,000 kg/hr, or about 13,000 kg/hr to about 16,000 kg/hr, about 20,000 kg/hr, about 25,000 kg/hr, or about 30,000 kg/hr of the mixture can be recovered from the blender. As the resinated furnish exits the blender, the resinated furnish can be deposited onto a conveyor belt and can be transported to one or more dryers, moistening systems, presses, and/or other processing equipment. For example, a particleboard product can be made blending a first or “face” mixture and a second or “core” mixture in a first and second blend, respectively. The first blender can produce about 13,600 kg/hr to about 15,900 kg/hr of a “face” mixture and the second blender can produce about 18,100 kg/hr to about 20,400 kg/hr of a “core” mixture. The “face” and “core” mixtures can be used to produce a particleboard panel or sheet, where the “face” mixture makes up the outer layers of the particleboard and the “core” mixture makes up the inner or core layer of the particleboard.

Referring to particleboard in particular, particleboard made according to one or more embodiments discussed and described herein can meet or exceed the requirements for H-1, H-2, H-3, M-0, M-1, M-S, M-2, M-3i, LD-1, and/or LD-2 grade particleboard as described in the American National Standards Institute (ANSI) for particleboard, i.e., ANSI A208.1-2009 Particleboard, approved Feb. 2, 2009. Particleboard made according to one or more embodiments discussed and described herein can meet or exceed the requirements for PBU, D-2, D-3, and/or M-3 as defined by the ANSI for particleboard, i.e., ANSI A208.1-2009 Particleboard, approved Feb. 2, 2009. For example, Tables A and B set out certain requirements for the different grades of particleboard. Referring to oriented strand board (OSB) in particular, OSB made according to one or more embodiments discussed and described herein can meet or exceed the U.S. Department of Commerce Voluntary Performance Standard PS 2. Referring to plywood in particular, plywood made according to one or more embodiments discussed and described herein can meet or exceed the U.S. Department of Commerce Voluntary Performance Standard PS 1 and/or PS-2.

Composite products in the shape or form of a panel, sheet, board, or the like can be in the form of a rectangular prism that includes six outer surfaces, e.g., three pairs of oppositely facing surfaces. The first pair of oppositely facing surfaces of the composite product can include a first or “top” surface and an opposing second or “bottom” surface. The second and third pairs of oppositely facing surfaces of the composite product can be referred to as the “side surfaces” that have a surface area less than the surface area of the first and second surfaces. As such, composite products in the shape or form of a panel, sheet, board, or the like can have an average thickness, where the average thickness is the length or distance between the first and second surfaces.

Pressure can optionally be applied to the resinated furnish before, during, and/or after the resinated furnish is heated to produce the composite product. For example, if the desired composite product shape or structure is a panel, sheet, board, or the like, an amount of the mixture sufficient to produce a composite product of the desired size and having the desired dimensions, can be transported, directed, placed, introduced, disposed, or otherwise located within a press capable of pressing the mixture before the mixture is heated and/or when the mixture is heated. The press can be an open press or a closed press.

Illustrative open presses can be as discussed and described in U.S. Pat. Nos. 4,017,248; 5,337,655; 5,611,269; 5,950,532; 6,098,532; and 6,782,810. Suitable, commercially available, open presses can include, but are not limited to, the CONTIROLL® press available from Siempelkamp and the CPS press available from Dieffenbacher.

In one or more embodiments, the resinated furnish can be pressed between at least two surfaces in a press and the binder in the resinated furnish can be at least partially cured to produce the composite product. At least one of the at least two press surfaces can be porous, i.e., can be or include a porous surface. In some examples, the at least two press surfaces can have at least one porous surface and can have at least one nonporous surface. In other examples, the at least two press surfaces can be or include two porous surfaces. During the pressing and heating of the resinated furnish to produce the composite product, steam can be generated from the resinated furnish and can be emitted through one or more porous surfaces.

In some configurations, the at least two press surfaces can include a first facial contact surface and a second facial contact surface. The resinated furnish can be heated and pressed to produce the composite product that can have a first face opposite of a second face. The first facial contact surface can make contact and apply pressure to the first face of the resinated furnish to produce the first face of the composite product. Similarly, the second facial contact surface can make contact and apply pressure to the second face of the resinated furnish to produce the second face of the composite product.

The porous surface can be or include a screen or a mesh, such as, but not limited to, a press screen, a caul screen, a caul plate, a mesh screen, a press weave, a perforated platen (e.g., perforated hot press platen), a press belt, a porous conveyor belt, a mesh belt, a screen belt, or any combination thereof. The porous surface can have a plurality of holes, slits, openings, apertures, or orifices that can be the same size or of different sizes therethrough.

The porous surface can be manufactured from and/or include high-tensile steel, carbon steel, stainless steel, titanium, nickel, chromium, tungsten, a hybrid mesh of carbon steel and stainless steel, alloys thereof, or combinations thereof. In some examples, the porous surface can include one or more meshes that have a twilled weave pattern or a plain weave pattern.

The porous surface can have 1, 2, 3, or 5 openings per linear centimeter to 6, 10, about 12, about 15, or about 25 openings per linear centimeter. For example, the porous surface can have 1 to about 24 openings per linear centimeter, 1 to about 20 openings per linear centimeter, 1 to about 14 openings per linear centimeter, 1 to about 10 openings per linear centimeter, 1 to about 8 openings per linear centimeter, 1 to about 6 openings per linear centimeter, 2 to about 24 openings per linear centimeter, 2 to about 20 openings per linear centimeter, 2 to about 14 openings per linear centimeter, 2 to about 10 openings per linear centimeter, 2 to about 8 openings per linear centimeter, 2 to about 6 openings per linear centimeter, 4 to about 24 openings per linear centimeter, 4 to about 20 openings per linear centimeter, 4 to about 14 openings per linear centimeter, 4 to about 10 openings per linear centimeter, 4 to about 8 openings per linear centimeter, or 4 to about 6 openings per linear centimeter.

In some examples, each opening through the porous surface can have a mesh size of about 250, about 200, about 180, about 150, or about 120 to about 100, about 80, about 60, about 50, about 40, about 20, about 10, or about 6. For example, each opening through the porous surface can have a mesh size of about 220 to about 8, about 200 to about 8, about 120 to about 8, about 80 to about 8, about 50 to about 8, about 18 to about 8, about 220 to about 18, about 200 to about 18, about 120 to about 18, about 80 to about 18, about 50 to about 18, or about 25 to about 18.

In one or more examples, the porous surface can have openings with the size of about 80 mesh and can have six openings per linear centimeter. In some examples, the porous surface can have openings with the size of about 60 mesh and can have six openings per linear centimeter. In other examples, the porous surface can have openings with the size of about 35 mesh and can have five openings per linear centimeter. In some examples, the porous surface can have openings with the size of about 18 mesh and can have five openings per linear centimeter.

Illustrative porous surfaces suitable for hot presses, can include, but are not limited to, the Planoflex caul screen or press screen, commercially available from Andritz, Inc., and the Flexoplan caul screen or press screen, commercially available from GKD-USA, Inc.

During the process to cure the binder and produce the composite product, the press and/or at least one or two press surfaces can be heated to a temperature of about 100° C., about 110° C., about 120° C., about 135° C., or about 150° C. to about 160° C., about 175° C., about 185° C., about 195° C., about 200° C., about 225° C., or about 250° C. For example, the press and/or at least one or two press surfaces can be heated to a temperature of about 110° C. to about 220° C., about 140° C. to about 180° C., about 145° C. to about 170° C., or about 149° C. to about 166° C.

Heat from the press and/or at least one or two press surfaces can be transferred to the resinated furnish to produce the composite product. During the pressing, resinated furnish, the at least partially cured resinated furnish, and/or the composite product can be heated and pressed by the at least two surfaces until a core of the composite product has a maximum internal board temperature (T_(max)) and/or a maximum internal board pressure (P_(max)). Thereafter, the heating and/or pressing to the composite product can be ceased. The maximum internal board temperature of the composite product is less than the temperature of at least one or two press surfaces.

The maximum internal board temperature of the composite product can be about 100° C., about 105° C., about 110° C., about 115° C., or about 120° C. to about 125° C., about 130° C., about 135° C., about 140° C., about 145° C., about 150° C., about 155° C., about 160° C., about 165° C., or about 170° C., as measured at the core of the composite product. The maximum internal board temperature of the composite product can be about 100° C., about 105° C., about 110° C., about 115° C., or about 120° C. to less than 125° C., less than 130° C., less than 135° C., less than 140° C., less than 145° C., less than 150° C., less than 155° C., less than 160° C., or less than 165° C., as measured at the core of the composite product. For example, the maximum internal board temperature of the composite product can be about 100° C. to less than 165° C., about 100° C. to less than 160° C., about 100° C. to less than 155° C., about 100° C. to less than 150° C., about 100° C. to less than 148° C., about 100° C. to less than 144° C., about 100° C. to less than 142° C., about 100° C. to less than 140° C., about 100° C. to less than 138° C., about 100° C. to less than 134° C., about 100° C. to less than 132° C., about 100° C. to less than 127° C., about 100° C. to less than 124° C., about 100° C. to less than 121° C., about 112° C. to less than 148° C., about 112° C. to less than 144° C., about 112° C. to less than 142° C., about 112° C. to less than 140° C., about 112° C. to less than 138° C., about 112° C. to less than 134° C., about 112° C. to less than 132° C., about 112° C. to less than 127° C., about 112° C. to less than 124° C., or about 112° C. to less than 121° C., as measured at the core of the composite product.

The maximum internal board pressure of the composite product can be about 0.01 MPa, about 0.03 MPa, about 0.05 MPa, about 0.07 MPa, about 0.09 MPa, or about 0.1 MPa to about 0.12 MPa, about 0.15 MPa, about 0.18 MPa, about 0.2 MPa, about 0.25 MPa, about 0.3 MPa, about 0.35 MPa, about 0.4 MPa, about 0.45 MPa, about 0.5 MPa, about 0.55 MPa, or about 0.6 MPa, as measured at the core of the composite product. In some examples, the maximum internal board pressure of the composite product can be about 0.01 MPa, about 0.03 MPa, about 0.05 MPa, about 0.07 MPa, about 0.09 MPa, or about 0.1 MPa to less than 0.12 MPa, less than 0.15 MPa, less than 0.18 MPa, less than 0.2 MPa, less than 0.25 MPa, less than 0.3 MPa, less than 0.35 MPa, less than 0.4 MPa, less than 0.45 MPa, less than 0.5 MPa, less than 0.55 MPa, or less than 0.6 MPa, as measured at the core of the composite product. For example, the maximum internal board pressure of the composite product can be about 0.01 MPa to about 0.37 MPa, about 0.01 MPa to about 0.33 MPa, about 0.01 MPa to about 0.27 MPa, about 0.01 MPa to about 0.22 MPa, about 0.01 MPa to about 0.17 MPa, about 0.05 MPa to about 0.37 MPa, about 0.05 MPa to about 0.33 MPa, about 0.05 MPa to about 0.27 MPa, about 0.05 MPa to about 0.22 MPa, about 0.05 MPa to about 0.17 MPa, about 0.01 MPa to less than 0.37 MPa, about 0.01 MPa to less than 0.33 MPa, about 0.01 MPa to less than 0.27 MPa, about 0.01 MPa to less than 0.22 MPa, about 0.01 MPa to less than 0.17 MPa, about 0.05 MPa to less than 0.37 MPa, about 0.05 MPa to less than 0.33 MPa, about 0.05 MPa to less than 0.27 MPa, about 0.05 MPa to less than 0.22 MPa, or about 0.05 MPa to less than 0.17 MPa, as measured at the core of the composite product.

One or more probes can be placed in the center or core of the resinated furnish prior to curing the resin such that after at least partially curing the resin, the probe is at the core of the composite product. The internal board temperatures and the internal board pressures can be monitored before the pressing, during the pressing, and/or after the pressing by a press probe monitoring system. The pressing can be stopped upon reaching the maximum internal board temperature and/or the maximum internal board pressure. An illustrative monitoring system suitable for measuring, recording, and/or monitoring the internal board temperatures and/or the internal board pressures, can include, but is not limited to, the PRESSMAN® press probe monitoring system, commercially available from Alberta Innovates Technology Futures, Edmonton, Alberta.

In some examples, at least one or two press surfaces can be heated to a first temperature, and the core of the composite product can be heated by the at least two press surfaces to a second temperature that is less than the first temperature. For example, the at least two press surfaces can be heated to the first temperature of 110° C. to about 180° C. and the core of the composite product can be heated by the at least two press surfaces to the second temperature (T_(max)) of about 100° C. to about 165° C.

In other examples, when the resinated furnish is heated and pressed between the at least two press surfaces, steam can be generated or otherwise produced from water contained in the resinated furnish. The water can be derived from the lignocellulose substrates, the binder, and/or other components of the resinated furnish. As the core of the composite product reaches the T_(max) and/or the P_(max), the steam can be emitted through at least one of the press surfaces, at least two of the press surfaces, or more press surfaces. Steam can also be emitted through at least one, two, three, or four edge surfaces of the resinated furnish and/or the composite product.

In one or more embodiments, if the composite product is in the form of a panel, sheet, board, or the like, the amount or length of time the resinated furnish can be heated can be about 5 seconds per millimeter (s/mm), about 10 s/mm, about 12 s/mm, or about 15 s/mm to about 17 s/mm, about 19 s/mm, about 21 s/mm, about 23 s/mm, about 25 s/mm, about 27 s/mm, about 30 s/mm, about 35 s/mm, about 40 s/mm, about 50 s/mm, or about 60 s/mm, where the length refers to the average thickness of the composite product. For example, the resinated furnish can be heated for a time of about 5 s/mm to about 55 s/mm, about 10 s/mm to about 45 s/mm, about 15 s/mm to about 40 s/mm, about 5 s/mm to about 25 s/mm, about 7 s/mm to about 27 s/mm, about 9 s/mm to about 24 s/mm, about 11 s/mm to about 22 s/mm, about 8 s/mm to about 20 s/mm, about 14 s/mm to about 18 s/mm, about 6 s/mm to about 14 s/mm, about 10 s/mm to about 18 s/mm, or about 10 s/mm to about 16 s/mm, where the length refers to the average thickness of the composite product. In another example, the resinated furnish can be heated for a time less than 120 s/mm, less than 110 s/mm, less than 100 s/mm, less than 90 s/mm, less than 80 s/mm, less than 70 s/mm, less than 60 s/mm, less than 50 s/mm, less than 40 s/mm, less than 30 s/mm, less than 25 s/mm, less than 22 s/mm, less than 20 s/mm, less than 18 s/mm, less than 17 s/mm, less than 16 s/mm, less than 15 s/mm, less than 14 s/mm, less than 13 s/mm, or less than 12 s/mm, where the length refers to the average thickness of the composite product.

In one specific example, a composite product in the form of a panel, sheet, board, or the like and having an average thickness of about 15 mm and subjected to a total heating time of about 4 minutes would correspond to heating the mixture for about 16 s/mm. In one or more examples, the resinated furnish can be heated to a temperature of about 160° C. to about 170° C. for a time of about 10 s/mm to about 30 s/mm, about 13 s/mm to about 19 s/mm, about 15 s/mm to about 40 s/mm, or about 8 s/mm to about 50 s/mm.

In other examples, an open press can be used to press the mixture when the mixture is heated, e.g., to a temperature of about 100° C. to about 250° C. In another example, the mixture can be extruded through a die (extrusion process) and heated to produce the composite product. The mixture can be pressed under a pressure of about 0.5 MPa, about 1 MPa, about 3 MPa, or about 5 MPa to about 7 MPa, about 9 MPa, or about 11 MPa.

The composite product can have a density of about 0.5 g/cm³, about 0.55 g/cm³, about 0.6 g/cm³, about 0.63 g/cm³, about 0.65 g/cm³, about 0.67 g/cm³, or about 0.7 g/cm³ to about 0.75 g/cm³, about 0.77 g/cm³, about 0.8 g/cm³, about 0.83 g/cm³, about 0.85 g/cm³, about 0.88 g/cm³, about 0.93 g/cm³, about 0.97 g/cm³, about 1 g/cm³, about 1.05 g/cm³, about 1.1 g/cm³, about 1.15 g/cm³, or about 1.2 g/cm³. For example, the composite product can have a density of about 0.7 g/cm³ to about 0.75 g/cm³, about 0.65 g/cm³ to about 0.85 g/cm³, about 0.65 g/cm³ to about 0.8 g/cm³, about 0.67 g/cm³ to about 0.77 g/cm³, about 0.5 g/cm³, to about 1 g/cm³, about 0.5 g/cm³, to about 0.8 g/cm³, about 0.5 g/cm³ to about 0.75 g/cm³, or about 0.64 g/cm³ to about 0.8 g/cm³. In one or more embodiments, the composite product can have density less than 1 g/cm³, less than 0.95 g/cm³, less than 0.88 g/cm³, less than 0.85 g/cm³, less than 0.83 g/cm³, less than 0.8 g/cm³, less than 0.79 g/cm³, less than 0.78 g/cm³, less than 0.77 g/cm³, less than 0.76 g/cm³, less than 0.75 g/cm³, less than 0.74 g/cm³, or less than 0.73 g/cm³.

The composite product can have an internal bond strength of about 0.1 MPa, about 0.2 MPa, about 0.3 MPa, about 0.35 MPa, about 0.4 MPa, about 0.5 MPa, about 0.6 MPa, about 0.7 MPA, about 0.8 MPa, about 0.9 MPa, about 1 MPa, or about 1.1 MPa to about 1.5 MPa, about 2 MPa, about 2.5 MPa, about 3 MPa, about 3.5 MPa, about 4 MPa, or about 5 MPa. For example, the composite product can have an internal bond strength of about 0.35 MPa to about 5.5 MPa, about 0.4 MPa to about 4.6 MPa, about 0.48 MPa to about 3.8 MPa, about 0.6 MPa to about 3.2 MPa, about 0.8 MPa to about 2.6 MPa, or about 0.5 MPa to about 2.1 MPa. In another example, the composite product can have an internal bond strength of about 0.5 MPa to about 2 MPa, about 0.6 MPa to about 1.6 MPa, about 1 MPa to about 1.7 MPa, about 0.6 MPa to about 1.2 MPa, or about 0.55 MPa to about 1.5 MPa. In one or more embodiments, the composite product can have an internal bond strength of at least 0.3 MPa, at least 0.33 MPa, at least 0.35 MPa, at least 0.38 MPa, at least 0.41 MPa, at least 0.45 MPa, at least 0.48 MPa, at least 0.51 MPa, at least 0.55 MPa, at least 0.58 MPa, at least 0.62 MPa, at least 0.65 MPa, at least 0.69 MPa, at least 0.72 MPa, at least 0.76 MPa, or at least 0.79 MPa. The internal bond strength for each example can be determined according to the Standard Test Methods for Evaluating Properties of Wood-Base Fiber and Particle Panel Materials, ASTM D1037-12, commercially available from ASTM International, Inc.

In one or more embodiments, the composite product can have a density less than 1 g/cm³, less than 0.95 g/cm³, less than 0.9 g/cm³, less than 0.85 g/cm³, less than 0.8 g/cm³, less than 0.79 g/cm³, less than 0.78 g/cm³, less than 0.77 g/cm³, less than 0.76 g/cm³, less than 0.75 g/cm³, less than 0.74 g/cm³, or less than 0.73 g/cm³ and an internal bond strength of at least 0.3 MPa, at least 0.35 MPa, at least 0.4 MPa, at least 0.48 MPa, at least 0.51 MPa, at least 0.55 MPa, at least 0.58 MPa, at least 0.62 MPa, at least 0.65 MPa, or at least 0.69 MPa. In one or more examples, the composite product can have a density less than 0.8 g/cm³ and internal bond strength of at least 0.48 MPa. In some examples, the composite product can have a density less than 0.8 g/cm³ and internal bond strength of at least 0.69 MPa. In other examples, the composite product can have a density of less than 0.73 g/cm³ and internal bond strength of at least 0.48 MPa. In other examples, the composite product can have a density of less than 0.73 g/cm³ and internal bond strength of at least 0.58 MPa.

In one or more embodiments, the composite product can have a density of about 0.65 g/cm³, about 0.68 g/cm³, about 0.7 g/cm³, about 0.72 g/cm³, about 0.74 g/cm³, about 0.75 g/cm³, about 0.77 g/cm³, or about 0.79 g/cm³ to about 0.8 g/cm³, about 0.82 g/cm³, about 0.84 g/cm³, about 0.85 g/cm³, about 0.88 g/cm³, about 0.9 g/cm³, about 0.92 g/cm³, about 0.95 g/cm³, about 0.97 g/cm³, about 1 g/cm³, about 1.05 g/cm³, or about 1.1 g/cm³, and an internal bond strength of at least 0.3 MPa, at least 0.35 MPa, at least 0.4 MPa, at least 0.48 MPa, at least 0.51 MPa, at least 0.55 MPa, at least 0.58 MPa, at least 0.62 MPa, or at least 0.65 MPa to about 0.67 MPa, about 0.69 MPa, about 0.7 MPa, about 0.75 MPa, about 0.8 MPa, about 0.85 MPa, about 0.9 MPa, about 0.95 MPa, about 1 MPa, about 1.1 MPa, about 1.2 MPa, about 1.5 MPa, or greater. In one or more examples, the composite product can have an internal bond strength of at least 0.35 MPa to about 1 MPa and a density of about 0.7 g/cm³ to about 0.9 g/cm³.

Composite products such as particleboard, fiberboard, plywood, and oriented strand board, can have a thickness or average thickness of about 1.5 mm, about 5 mm, or about 10 mm to about 15 mm, about 20 mm, about 25 mm, about 30 mm, about 50 mm, about 100 mm, about 200 mm, or about 300 mm. Composite products such as particleboard, fiberboard, plywood, and oriented strand board can have a length of about 0.1 m, about 0.5 m, about 1 m, about 1.2 m, about 1.8 m, about 2.4 m, about 3 m, or about 3.6 m. The composite products can also have a width of about 0.1 m, about 0.5 m, about 1 m, about 1.2 m, about 1.8 m, about 2.4 m, or about 3 m.

The mixtures discussed and described herein can be free or essentially free of formaldehyde for use in the production of the composite products, e.g., wood products such as particleboard and plywood. As used herein, the term “essentially free of formaldehyde” means the mixture does not include or contain any intentionally added formaldehyde or compounds that can decompose, react, or otherwise form formaldehyde. Said another way, the term “essentially free of formaldehyde” means the mixture does not contain formaldehyde or compounds that can form formaldehyde, but may include formaldehyde present as an impurity. Accordingly, depending on the particular multifunctional aldehydes used to produce the mixtures discussed and described herein, the mixture can be referred to as a “no added formaldehyde” or “NAF” mixture.

The composite products discussed and described herein can exhibit a low level of formaldehyde emission. A suitable test for determining formaldehyde emission from a composite product can include ASTM D6007-02 and AST E1333-10. For example, the composite products can exhibit a formaldehyde emission of zero. In another example, the composite products can exhibit a formaldehyde emission of less than 1 part per million (“ppm”), less than 0.9 ppm, less than 0.08 ppm, less than 0.07 ppm, less than 0.06 ppm, less than 0.05 ppm, less than 0.04 ppm, less than 0.03 ppm, less than 0.02 ppm, less than 0.01 ppm, or less than 0.005 ppm.

The composite product can meet or exceed the formaldehyde emission standards required by the California Air Resources Board (“CARB”) Phase 1 (less than 0.1 parts per million “ppm” formaldehyde for particleboard), and Phase 2 (less than 0.09 ppm formaldehyde for particleboard). The composite products discussed and described herein can also meet or exceed the formaldehyde emission standards required by the Japanese JIS/JAS F*** (does not exceed 0.5 mg/L formaldehyde for particleboard), Japanese JIS/JAS F**** (does not exceed 0.3 mg/L formaldehyde for particleboard), European E1, and European E2 standards.

EXAMPLES

In order to provide a better understanding of the foregoing discussion, the following non-limiting examples are offered. Although the examples may be directed to specific embodiments, they are not to be viewed as limiting the invention in any specific respect. All parts, proportions, and percentages are by weight unless otherwise indicated.

The binder composition of Examples 1-4 was a mixture of: Prepolymer 1 (unsaturated compound), ammonium lignosulfonate (polyphenolic compound), and hydrogen peroxide (free radical precursor) and was used to make four particleboard panels. The binder composition of Example 5 was a mixture of: Prepolymer 2 (unsaturated compound), ammonium lignosulfonate (polyphenolic compound), and hydrogen peroxide (free radical precursor) and was used to make one particleboard panel. Prepolymers 1 and 2 were used to make the particleboard panels within 24 hr after preparation.

Preparation of Prepolymer 1

Prepolymer 1 was synthesized from glycerol and itaconic acid according to the following procedure. To a 1 L glass reactor, itaconic acid (about 800 g or about 6.15 moles, sample from Cargill), glycerol (about 800 g or about 8.69 moles, purchased from Sigma-Aldrich Co.), Bu₂SnO catalyst (about 1.6 g of Fascat 4201, purchased from Archema, Inc.), and hydroquinone (about 1.6 g, purchased from Sigma-Aldrich Co.) were added. The reactor was equipped with a mechanical stirrer, a thermocouple, a moisture-trap with a three-way stopcock, and a cold-finger reflux condenser. The reaction was conducted under a constant nitrogen purge. Over the course of 1 hr, the flask was heated from room temperature (e.g., about 25° C.) to about 182° C. where water began collecting in the moisture trap. The reaction mixture was further heated over the next hour to a temperature of about 202° C., at which point about 174.5 g of condensate water had been collected. The reaction mixture was cooled using an ice bath to less than 100° C., and the reaction mixture was mixed with about 533 g of 50% hydrogen peroxide (purchased from Degussa) and stored in a plastic container.

Preparation of Prepolymer 2

Prepolymer 2 was synthesized from pentaerythritol and maleic anhydride according to the following procedure. To a 2 L glass reactor, maleic anhydride (about 577 g or about 5.9 mol, purchased from Acros Organics) and pentaerythritol (about 545 g or about 4.0 mol, purchased from Acros Organics) were added. The glass reactor was equipped with a mechanical stirrer, a thermocouple, and a reflux condenser. The reactor was heated from room temperature (e.g., about 25° C.) to about 55° C. over 40 min at which point maleic anhydride started to melt. An additional amount of maleic anhydride (about 600 g or about 6.1 mol) was added and the reaction temperature was raised from about 55° C. to about 120° C. over 1 hr. The reaction was stirred at about 120° C. for additional 1 hr, at which point reaction mixture gradually started to turn into a light yellow solution and was then cooled in air to less than 100° C. After the reaction mixture was cooled, water was added to make an about 80 wt % solution.

Preparation of Particleboard Panels for Examples 1-5

Face-grade particleboard wood furnish in the amount of about 2,100 g of southern yellow pine that had a moisture content of about 5 wt % to about 7 wt % was placed in blender. While blending, the components of the binder were applied in the form of a fine mist in the following order: a) about 5 wt % to about 6 wt % of ammonium lignosulfonate (about 46 wt % to about 49 wt % aq.) mixed with about 0.1 wt % of FeSO₄; b) about 3.0 wt % to about 4 wt % of Prepolymer 1 or 2 (about 70 wt % to about 80 wt % aq.); and c) 0.6 wt % to 5.6 wt % of hydrogen peroxide (50 wt % aq.). The resinated furnish or mixture (moisture content of about 12 wt % to about 17 wt %) was blended for an additional 2 min.

The resinated furnish was formed into a mat having the dimensions of about 40.64 cm×about 40.64 cm×about 5.08 cm. The mat was pressed for about 4 min at a temperature of about 165.5° C. (total press time of about 240 sec included about 30 sec closing time, about 180 sec press time at about 8.27 MPa, and about 30 sec degas time) to produce a panel having thickness of about 1.58±0.2 cm. Final particleboard panels were cooled to room temperature (e.g., about 25° C.) and the internal bond (TB) strengths were tested. Table 1 below shows the particular amount of each component combined with the wood furnish and the product properties for Examples 1-5.

TABLE 1 Loading ODW (wt %) Density IB Ex Prepolymer Prepolymer FeSO₄ H₂O₂ ALS (g/cm³) (MPa) 1 1 3.5 0.1 5.6 6.0 0.79 0.68 2 1 4.0 0.1 0.6 6.0 0.77 0.39 3 1 4.0 0.1 2.6 6.0 0.83 1.10 4 1 3.0 0.1 3.5 5.0 0.8 0.59 5 2 3.0 0.1 2.0 5.0 0.79 0.60

The binder of Examples 6-9 was a mixture of: Prepolymer 3 (unsaturated compound), ammonium lignosulfonate (polyphenolic compound), and hydrogen peroxide (free radical precursor) and was used to make four particleboard panels. Prepolymer 3 was used to make the particleboard panels within 24 hr after preparation. The particleboard panels were produced with the dimensions of about 61.0 cm×about 61.0 cm×about 1.6 cm in Examples 6 and 7 and about 121.9 cm×about 243.8 cm×about 1.6 cm in Examples 8 and 9. Table 2 below shows the particular pressing conditions and panel properties for Examples 6-9.

Preparation of Prepolymer 3

Prepolymer 3 was synthesized from pentaerythritol and maleic anhydride according to the following procedure. To a 3.8 L reactor, maleic anhydride (about 205.8 g or about 2.1 mol, purchased from Acros Organics) and pentaerythritol (about 95.2 g or about 0.7 mol, purchased from Acros Organics) were added. The reactor was equipped with a mechanical stirrer, a thermocouple, and a reflux condenser. The reactor was heated from room temperature (e.g., about 25° C.) to about 120° C. over the course of about 45 min. Heating was then discontinued and the reaction mixture exothermed to a temperature of about 180° C. to about 190° C. The reaction mixture cooled in air to a temperature of less than 100° C. Then diethylene glycol (about 200 g, purchased from Sigma-Aldrich Co.) was added to the cooled mixture to produce a 60 wt % mixture.

Preparation of Resinated Furnish for Examples 6-9

Face-grade particleboard wood furnish in the amount of about 27.1 kg of southern yellow pine substrates that had a moisture content of about 5 wt % to about 8 wt % was placed in blender. The components of the binder were pre-blended prior to being applied to the substrates in the form of a fine mist. The components of the binder were combined in the following amounts: a) about 60 wt % to about 68 wt % of Prepolymer 3 (about 58 wt % to about 62 wt % in diethylene glycol) mixed with b) about 2.9 wt % of FeEDTA (about 10 wt % aq.) and c) about 30 wt % to about 35 wt % of hydrogen peroxide (about 50 wt % aq.). The resinated furnish (moisture content of about 11.7 wt % to about 16.5 wt %) was blended for about an additional 2 min.

Core-grade particleboard wood furnish in the amount of about 30.1 kg of southern yellow pine substrates that had a moisture content of about 3 wt % to about 6 wt % was placed in blender. The components of the binder were pre-blended prior to being applied to the substrates in the form of a fine mist. The components of the binder were combined in the following amounts: a) about 60 wt % to about 68 wt % of Prepolymer 3 (about 58 wt % to about 62 wt % in diethylene glycol) mixed with b) about 2.9 wt % of FeEDTA (about 10 wt % aq.) and c) about 30 wt % to about 35 wt % of hydrogen peroxide (about 50 wt % aq.). The resinated furnish (moisture content of about 8.4 wt % to about 14.2 wt %) was blended for about an additional 2 min.

The three-layer particleboard was constructed using a weight ratio of 22.5% face/55% core/22.5% face resinated furnish.

Preparation of Particleboard Panels for Example 6

The resinated furnish from above with an average moisture content of about 9.9 wt % was formed into a mat having the dimensions of about 61.0 cm×about 61.0 cm×about 5.1 cm. The mat was placed in a Dieffenbacher press having two nonporous cauls, each caul formed from a nonporous TEFLON® sheet. Hot press probes were placed in the center of the mat to monitor the internal board temperatures and the internal board pressures during the pressing. The press temperature was at about 149° C. The mat was pressed for about 165 sec (total press time was from closing time to final thickness reached in press time) to produce a particleboard panel having the dimensions of about 61.0 cm×about 61.0 cm×about 1.6 cm and a density of about 0.795 g/cm³. During the pressing, a maximum internal board temperature (T_(max)) of about 148° C. and a maximum internal board pressure (P_(max)) of about 0.26 MPa were recorded using a PRESSMAN® press probe monitoring system (available from Alberta Innovates Technology Futures, Edmonton, Alberta). The final particleboard panel was cooled to room temperature (e.g., about 25° C.) and had an IB of about 0.90 MPa.

Preparation of Particleboard Panels for Example 7

The resinated furnish from above with an average moisture content of about 10.4 wt % was formed into a mat having the dimensions of about 61.0 cm×about 61.0 cm×about 5.1 cm. The mat was placed in a Dieffenbacher press having a Planoflex caul screen (commercially available from Andritz, Inc.). Hot press probes were placed in the center of the mat to monitor the internal board temperatures and the internal board pressures during the pressing. The press temperature was at about 149° C. The mat was pressed for about 80 sec (total press time was from closing time to final thickness reached in press time) to produce a particleboard panel having the dimensions of about 61.0 cm×about 61.0 cm×about 1.6 cm and a density of about 0.788 g/cm³. During the pressing, a maximum internal board temperature (T_(max)) of about 121° C. and a maximum internal board pressure (P_(max)) of about 0.05 MPa were recorded using a PRESSMAN® press probe monitoring system (available from Alberta Innovates Technology Futures, Edmonton, Alberta). The final particleboard panel was cooled to room temperature (e.g., about 25° C.) and had an IB of about 0.54 MPa.

Preparation of Particleboard Panels for Example 8

The resinated furnish from above with an average moisture content of about 15.0 wt % was formed into a mat having the dimensions of about 121.9 cm×about 243.8 cm×about 5.1 cm. The mat was placed in a Dieffenbacher press having two nonporous cauls, each caul formed from a nonporous TEFLON® sheet. Hot press probes were placed in the center of the mat to monitor the internal board temperatures and the internal board pressures during the pressing. The press temperature was at about 166° C. The mat was pressed for about 20 sec (total press time was from closing time to final thickness reached in press time) to produce a particleboard panel having the dimensions of about 121.9 cm×about 243.8 cm×about 1.6 cm and a density of about 0.811 g/cm³. During the pressing, a maximum internal board temperature (T_(max)) of about 149° C. and a maximum internal board pressure (P_(max)) of about 0.46 MPa were recorded using a PRESSMAN® press probe monitoring system (available from Alberta Innovates Technology Futures, Edmonton, Alberta). The final particleboard panel was cooled to room temperature (e.g., about 25° C.) and had an IB of about 0.44 MPa.

Preparation of Particleboard Panels for Example 9

The resinated furnish from above with an average moisture content of about 15.2 wt % was formed into a mat having the dimensions of about 121.9 cm×about 243.8 cm×about 5.1 cm. The mat was placed in a Dieffenbacher press having a Planoflex caul screen (commercially available from Andritz, Inc.). Hot press probes were placed in the center of the mat to monitor the internal board temperatures and the internal board pressures during the pressing. The press temperature was at about 166° C. The mat was pressed for about 20 sec (total press time was from closing time to final thickness reached in press time) to produce a particleboard panel having the dimensions of about 121.9 cm×about 243.8 cm×about 1.6 cm and a density of about 0.819 g/cm³. During the pressing, a maximum internal board temperature (T_(max)) of about 132° C. and a maximum internal board pressure (P_(max)) of about 0.17 MPa were recorded using a PRESSMAN® press probe monitoring system (available from Alberta Innovates Technology Futures, Edmonton, Alberta). The final particleboard panel was cooled to room temperature (e.g., about 25° C.) and had an IB of about 0.70 MPa.

TABLE 2 Press Internal Internal Panel Press Binder MC of Close Board Board Caul Density Temp Loading Mat Time Tmax Pmax IB Ex Type (g/cm³) (° C.) (% ODW) (wt %) (s) (° C.) (MPa) (MPa) 6 nonporous 0.795 149 6.18 9.9 165 148 0.26 0.90 7 porous 0.788 149 6.18 10.4 80 121 0.05 0.54 8 nonporous 0.811 166 6.18 15.0 20 149 0.46 0.44 9 porous 0.819 166 6.18 15.2 20 132 0.17 0.70

Embodiments of the present disclosure further relate to any one or more of the following paragraphs:

1. A binder composition, comprising: at least one polyphenolic compound; at least one unsaturated compound having two or more unsaturated carbon-carbon bonds, wherein at least one of the unsaturated carbon-carbon bonds is a pi-bond that is not conjugated with an aromatic moiety and is capable of free radical addition; and at least one free radical precursor.

2. A binder composition, comprising: at least one polyphenolic compound; at least one unsaturated compound having two or more unsaturated carbon-carbon bonds, wherein at least one of the unsaturated carbon-carbon bonds is a pi-bond that is not conjugated with an aromatic moiety and is capable of free radical addition; at least one oxidant; and at least one catalyst.

3. A binder composition, comprising: at least one polyphenolic compound; at least one unsaturated compound having two or more unsaturated carbon-carbon bonds, wherein at least one of the unsaturated carbon-carbon bonds is a pi-bond that is not conjugated with an aromatic moiety and is capable of free radical addition; and at least one free radical precursor comprising potassium ferricyanide, an iron complex of (S,S)-ethylenediamine-N,N′-disuccinic acid, an iron complex of ethyleneglycol bis(2-aminoethylether)-N,N,N′,N′-tetraacetic acid, an iron complex of trans-1,2-diaminocyclohexanetetraacetic acid, an iron complex of nitrilotriacetic acid (NTA), or any mixture thereof.

4. A method for making a composite product, comprising: combining a plurality of lignocellulose substrates, at least one polyphenolic compound, at least one unsaturated compound, and at least one free radical precursor to produce a mixture, wherein the unsaturated compound has two or more unsaturated carbon-carbon bonds, and wherein at least one of the unsaturated carbon-carbon bonds is a pi-bond that is not conjugated with an aromatic moiety and is capable of free radical addition; and heating the mixture to a temperature of about 60° C. to about 300° C. to produce a composite product.

5. A method for making a composite product, comprising: contacting a plurality of lignocellulose substrates with a binder composition comprising at least one polyphenolic compound, at least one unsaturated compound, and at least one free radical precursor to produce a mixture, wherein the unsaturated compound has two or more unsaturated carbon-carbon bonds, and wherein at least one of the unsaturated carbon-carbon bonds is a pi-bond that is not conjugated with an aromatic moiety and is capable of free radical addition; and at least partially curing the binder composition to produce a composite product.

6. A method for making a composite, comprising: combining a plurality of lignocellulose substrates with a binder composition, wherein the binder composition comprises at least one polyphenolic compound; at least one unsaturated compound, at least one oxidant; and at least one catalyst, wherein the unsaturated compound has two or more unsaturated carbon-carbon bonds, and wherein at least one of the unsaturated carbon-carbon bonds is a pi-bond that is not conjugated with an aromatic moiety and is capable of free radical addition.

7. A method for making a composite product, comprising: combining a plurality of lignocellulose substrates, at least one polyphenolic compound, at least one unsaturated compound, and at least one free radical precursor to produce a mixture, wherein the unsaturated compound has two or more unsaturated carbon-carbon bonds, wherein at least one of the unsaturated carbon-carbon bonds is a pi-bond that is not conjugated with an aromatic moiety and is capable of free radical addition, and wherein the free radical precursor is present in an amount of about 7 wt % to about 99 wt %, based on the weight of the one or more unsaturated compounds; and heating the mixture to a temperature of about 60° C. to about 300° C. to produce a composite product.

8. A method for making a composite product, comprising: contacting a plurality of lignocellulose substrates with a binder composition comprising at least one polyphenolic compound, at least one unsaturated compound, and at least one free radical precursor to produce a mixture, wherein the unsaturated compound has two or more unsaturated carbon-carbon bonds, and wherein at least one of the unsaturated carbon-carbon bonds is a pi-bond that is not conjugated with an aromatic moiety and is capable of free radical addition, and wherein the free radical precursor is present in an amount of about 7 wt % to about 99 wt %, based on the weight of the one or more unsaturated compounds; and at least partially curing the binder composition to produce a composite product.

9. A method for making a composite product, comprising: combining a plurality of lignocellulose substrates, at least one polyphenolic compound, at least one unsaturated compound, at least one oxidant, and at least on catalyst to produce a mixture, wherein the unsaturated compound has two or more unsaturated carbon-carbon bonds, wherein at least one of the unsaturated carbon-carbon bonds is a pi-bond that is not conjugated with an aromatic moiety and is capable of free radical addition; and heating the mixture to a temperature of about 60° C. to about 300° C. to produce a composite product, wherein at least 11 wt % of the oxidant present in the mixture is present when the mixture is heated to about 60° C. to about 300° C.

10. A method for making a composite product, comprising: combining a plurality of lignocellulose substrates, at least one polyphenolic compound, at least one unsaturated compound, and at least one free radical precursor to produce a mixture, wherein the unsaturated compound has two or more unsaturated carbon-carbon bonds, and wherein at least one of the unsaturated carbon-carbon bonds is a pi-bond that is not conjugated with an aromatic moiety and is capable of free radical addition, and wherein the free radical precursor comprises potassium ferricyanide, an iron complex of (S,S)-ethylenediamine-N,N′-disuccinic acid, an iron complex of ethyleneglycol bis(2-aminoethylether)-N,N,N′,N′-tetraacetic acid, an iron complex of trans-1,2-diaminocyclohexanetetraacetic acid, an iron complex of nitrilotriacetic acid (NTA), or any mixture thereof; and heating the mixture to a temperature of about 60° C. to about 300° C. to produce a composite product; and heating the mixture to a temperature of about 60° C. to about 300° C. to produce a composite product.

11. A composite product, comprising a plurality of lignocellulose substrates and an at least partially cured binder composition, wherein the binder composition, prior to at least partial curing, comprises: at least one polyphenolic compound; at least one unsaturated compound having two or more unsaturated carbon-carbon bonds, wherein at least one of the unsaturated carbon-carbon bonds is a pi-bond that is not conjugated with an aromatic moiety and is capable of free radical addition; and at least one free radical precursor.

12. A composite product, comprising a plurality of lignocellulose substrates and an at least partially cured binder composition, wherein the binder composition, prior to at least partial curing, comprises: at least one polyphenolic compound; at least one unsaturated compound having two or more unsaturated carbon-carbon bonds, wherein at least one of the unsaturated carbon-carbon bonds is a pi-bond that is not conjugated with an aromatic moiety and is capable of free radical addition; and at least one free radical precursor, wherein the free radical precursor is present in an amount of about 7 wt % to about 99 wt %, based on the weight of the one or more unsaturated compounds.

13. A composite product comprising a mixture that has been heated to a temperature of about 60° C. to about 300° C., wherein the mixture, prior to being heated, comprises a plurality of lignocellulose substrates, at least one polyphenolic compound, at least one unsaturated compound, and at least one free radical precursor, wherein the unsaturated compound has two or more unsaturated carbon-carbon bonds, and wherein at least one of the unsaturated carbon-carbon bonds is a pi-bond that is not conjugated with an aromatic moiety and is capable of free radical addition.

14. A composite product comprising a cured mixture of a plurality of lignocellulose substrates, at least one polyphenolic compound, at least one unsaturated compound, and at least one free radical precursor, wherein the unsaturated compound has two or more unsaturated carbon-carbon bonds, wherein at least one of the unsaturated carbon-carbon bonds is a pi-bond that is not conjugated with an aromatic moiety and is capable of free radical addition.

15. A composite product comprising a plurality of lignocellulose substrates and an at least partially cured binder composition, wherein the binder composition, prior to at least partial curing, comprises at least one polyphenolic compound, at least one unsaturated compound, and at least one free radical precursor, wherein the unsaturated compound has two or more unsaturated carbon-carbon bonds, wherein at least one of the unsaturated carbon-carbon bonds is a pi-bond that is not conjugated with an aromatic moiety and is capable of free radical addition, and wherein the free radical precursor comprises potassium ferricyanide, an iron complex of (S,S)-ethylenediamine-N,N′-disuccinic acid, an iron complex of ethyleneglycol bis(2-aminoethylether)-N,N,N′,N′-tetraacetic acid, an iron complex of trans-1,2-diaminocyclohexanetetraacetic acid, an iron complex of nitrilotriacetic acid (NTA), or any mixture thereof.

16. A composite product comprising a plurality of lignocellulose substrates and an at least partially cured binder composition, wherein the binder composition, prior to at least partial curing, comprises: at least one polyphenolic compound; at least one unsaturated compound, at least one oxidant; and at least one catalyst, wherein the unsaturated compound has two or more unsaturated carbon-carbon bonds, and wherein at least one of the unsaturated carbon-carbon bonds is a pi-bond that is not conjugated with an aromatic moiety and is capable of free radical addition.

17. The binder composition, method, or composite product according to any one of paragraphs 1 to 16, wherein the polyphenolic compound comprises one or more lignins, one or more tannins, one or more novolac resins, one or more bisphenols, one or more modified phenol formaldehyde resins, humic acid, or any mixture thereof.

18. The binder composition, method, or composite product according to any one of paragraphs 1 to 17, wherein the polyphenolic compound is modified with one or more compounds having carbon-carbon double bonds and one or more functional groups.

19. The binder composition, method, or composite product according to paragraph 18, wherein the one or more compounds having carbon-carbon double bonds and one or more functional groups comprises an unsaturated glycidyl ether, an unsaturated glycidyl ester, an unsaturated mono-epoxide, an unsaturated methylol compound, maleic anhydride, or any mixture thereof.

20. The binder composition, method, or composite product according to any one of paragraphs 1 to 19, wherein the one or more lignins is present and comprises ammonium lignosulfonate, sodium lignosulfonate, or a mixture thereof.

21. The binder composition, method, or composite product according to any one of paragraphs 1 to 20, wherein the unsaturated compound comprises dicyclopentadiene (DCPD), ethylene glycol diacrylate, ethylene glycol dimethacrylate, diethylene glycol diacrylate, diethylene glycol dimethacrylate, poly(ethylene glycol)diacrylate, poly(ethylene glycol)dimethacrylate, trimethylolpropane triacrylate (TMPTA), pentaerythritol tetraacrylate, pentaerythritol triacrylate, polyacrylate starch, linseed oil, an unsaturated prepolymer, or any mixture thereof.

22. The binder composition, method, or composite product according to any one of paragraphs 1 to 21, wherein the unsaturated compound comprises an unsaturated prepolymer, or any mixture thereof.

23. The binder composition, method, or composite product according to paragraph 22, wherein the unsaturated prepolymer comprises an unsaturated polyester prepolymer, an unsaturated polyether prepolymer; an unsaturated polyamide prepolymer, an unsaturated polyurethane prepolymer, or any mixture thereof.

24. The binder composition, method, or composite product according to paragraph 23, wherein the unsaturated polyester prepolymer is present.

25. The binder composition, method, or composite product according to paragraph 23, wherein the unsaturated polyether prepolymer is present.

26. The binder composition, method, or composite product according to paragraph 23, wherein the unsaturated polyamide prepolymer is present.

27. The binder composition, method, or composite product according to paragraph 23, wherein the unsaturated polyurethane prepolymer is present.

28. The binder composition, method, or composite product according to any one of paragraphs 23 to 27, wherein the unsaturated prepolymer is water soluble, water dispersible, or water emulsifiable.

29. The binder composition, method, or composite product according to any one of paragraphs 23 to 28, wherein the unsaturated prepolymer has a viscosity of about 20 cP to about 50,000 cP at a temperature of 25° C.

30. The binder composition, method, or composite product according to any one of paragraphs 1 to 29, wherein the at least one of the unsaturated carbon-carbon bonds that is a pi-bond that is not conjugated with an aromatic moiety and is capable of free radical addition is an α,β-unsaturated carbonyl.

31. The binder composition, method, or composite product according to any one of paragraphs 1 to 30, wherein the free radical precursor comprises a mixture of one or more oxidants and one or more catalysts.

32. The binder composition, method, or composite product according to any one of paragraphs 1 to 31, wherein the free radical precursor comprises a mixture of one or more inorganic oxidants and one or more catalysts.

33. The binder composition, method, or composite product according to any one of paragraphs 1 to 32, wherein the free radical precursor comprises a mixture of hydrogen peroxide and one or more iron containing catalysts.

34. The binder composition, method, or composite product according to any one of paragraphs 1 to 33, wherein the free radical precursor comprises a compound having the general formula R—N═N—R′, wherein R and R′ are independently a substituted aryl or a substituted alkyl.

35. The binder composition, method, or composite product according to any one of paragraphs 1 to 34, wherein the free radical precursor comprise azobisisobutyronitrile.

36. The binder composition, method, or composite product according to any one of paragraphs 1 to 35, wherein the one or more free radical precursors comprises one or more catalysts, and wherein the one or more catalysts comprises one or more metals in the form of a complex bound to one or more complexing agents.

37. The binder composition, method, or composite product according to paragraph 36, wherein the one or more complexing agents comprises cyanide (CN⁻), sulfate (SO₄ ²⁻), ethylenediaminetetraacetic acid (EDTA), ethylenediamine-N,N′-disuccinic acid (EDDS), ethyleneglycol bis(2-aminoethylether)-N,N,N′,N′-tetraacetic acid (EGTA), diethylenetriaminepentaacetic acid (DTPA), trans-1,2-diaminocyclohexane tetraacetic acid (CDTA), iminodisuccinate (IDS), nitrilotriacetic acid (NTA), or any mixture thereof.

38. The binder composition, method, or composite product according to paragraph 36, wherein the free radical precursor comprises one or more catalysts, and wherein the one or more catalysts comprises potassium ferricyanide, an iron complex of ethylenediaminetetraacetic acid, an iron complex of (S,S)-ethylenediamine-N,N′-disuccinic acid, an iron complex of diethylenetriamine pentaacetic acid, an iron complex of ethyleneglycol bis(2-aminoethylether)-N,N,N′,N′-tetraacetic acid, an iron complex of trans-1,2-diaminocyclohexanetetraacetic acid, or any mixture thereof.

39. The binder composition, method, or composite product according to any one of paragraphs 31 to 33 or 36 to 38, wherein the one or more catalysts comprises one or more metals.

40. The binder composition, method, or composite product according to any one of paragraphs 1 to 39, wherein the polyphenolic compound is present in an amount of at least 1 wt % to about 99 wt %, based on the combined weight of the polyphenolic compound, the unsaturated compound, and the free radical precursor.

41. The binder composition, method, or composite product according to any one of paragraphs 1 to 40, wherein the polyphenolic compound is present in an amount of at least 1 wt % to about 99 wt %, based on the combined weight of the polyphenolic compound and the unsaturated compound.

42. The binder composition, method, or composite product according to any one of paragraphs 1 to 41, wherein the unsaturated compound is present in an amount of at least 5 wt % to about 60 wt %, based on the combined weight of the polyphenolic compound, the unsaturated compound, and the free radical precursor.

43. The binder composition, method, or composite product according to any one of paragraphs 1 to 42, wherein the unsaturated compound is present in an amount of at least 5 wt % to about 65 wt %, based on the combined weight of the polyphenolic compound and the unsaturated compound.

44. The binder composition, method, or composite product according to any one of paragraphs 1 to 43, wherein the free radical precursor comprises a mixture of hydrogen peroxide and one or more catalysts, wherein the hydrogen peroxide is present in an amount of about 5 wt % to about 50 wt %, based on the combined weight of the polyphenolic compound, the unsaturated compound, and the free radical precursor, and wherein the one or more catalysts is present in an amount of about 0.1 wt % to about 5 wt %, based on the combined weight of the polyphenolic compound, the unsaturated compound, and the free radical precursor.

45. The binder composition, method, or composite product according to any one of paragraphs 1 to 44, wherein the free radical precursor comprises a mixture of hydrogen peroxide and one or more catalysts, wherein the hydrogen peroxide is present in an amount of about 15 wt % to about 35 wt %, based on the combined weight of the polyphenolic compound, the unsaturated compound, and the free radical precursor, and wherein the one or more catalysts is present in an amount of about 1 wt % to about 3 wt %, based on the combined weight of the polyphenolic compound, the unsaturated compound, and the free radical precursor.

46. The binder composition, method, or composite product according to any one of paragraphs 1 to 45, wherein the free radical precursor is present in an amount of about 10 wt % to about 300 wt %, based on the weight of the unsaturated compound.

47. The binder composition, method, or composite product according to any one of paragraphs 1 to 46, wherein the free radical precursor is present in an amount of about 60 wt % to about 100 wt %, based on the weight of the unsaturated compound.

48. The binder composition, method, or composite product according to any one of paragraphs 1 to 47, wherein the free radical precursor is present in an amount of about 5 wt % to about 200 wt %, based on the weight of the polyphenolic compound.

49. The binder composition, method, or composite product according to any one of paragraphs 1 to 48, wherein the free radical precursor is present in an amount of about 35 wt % to about 75 wt %, based on the weight of the polyphenolic compound.

50. The binder composition, method, or composite product according to any one of paragraphs 1 to 49, wherein the free radical precursor is present in an amount of about 5 wt % to about 70 wt %, based on the combined weight of the polyphenolic compound, the unsaturated compound, and the free radical precursor.

51. The binder composition, method, or composite product according to any one of paragraphs 1 to 50, wherein the free radical precursor is present in an amount of about 15 wt % to about 35 wt %, based on the combined weight of the polyphenolic compound, the unsaturated compound, and the free radical precursor.

52. The binder composition, method, or composite product according to any one of paragraphs 1 to 51, wherein the polyphenolic compound is present in the mixture in an amount of about 0.5 wt % to about 30 wt %, based on a dry weight of the plurality of lignocellulose substrates.

53. The binder composition, method, or composite product according to any one of paragraphs 1 to 52, wherein the polyphenolic compound is present in the mixture in an amount of about 3 wt % to about 9 wt %, based on a dry weight of the plurality of lignocellulose substrates.

54. The binder composition, method, or composite product according to any one of paragraphs 1 to 53, wherein the free radical precursor comprises one or more oxidants, and wherein at least 11 wt % of the oxidant is present when the mixture is heated to at least 60° C.

55. The binder composition, method, or composite product according to any one of paragraphs 1 to 54, wherein the free radical precursor comprises one or more oxidants, and wherein at least 15 wt % of the oxidant is present when the mixture is heated to at least 60° C.

56. The binder composition, method, or composite product according to any one of paragraphs 1 to 55, wherein the free radical precursor comprises one or more oxidants, and wherein at least 20 wt % of the oxidant is present when the mixture is heated to at least 60° C.

57. The binder composition, method, or composite product according to any one of paragraphs 1 to 56, wherein the free radical precursor comprises one or more oxidants, and wherein at least 50 wt % of the oxidant is present when the mixture is heated to at least 60° C.

58. The binder composition, method, or composite product according to any one of paragraphs 1 to 57, wherein an amount of the one or more free radical precursors present when the mixture is heated to about 60° C. to about 300° C. is at least 1 wt %, based on a dry weight of the plurality of lignocellulose substrates.

59. The binder composition, method, or composite product according to any one of paragraphs 1 to 58, wherein the free radical precursor is present in an amount of about 7 wt % to about 99 wt %, based on the weight of the unsaturated compound.

60. The binder composition, method, or composite product according to any one of paragraphs 1 to 59, wherein an amount of energy generated from the mixture due to exothermic reaction between two or more of the components of the mixture is less than 20 cal/g.

61. The binder composition, method, or composite product according to any one of paragraphs 1 to 60, wherein prior to heating the mixture to a temperature of about 60° C., an amount of energy generated from the mixture due to exothermic reaction(s) between the components of the mixture is less than 20 cal/g.

62. The binder composition, method, or composite product according to any one of paragraphs 1 to 61, wherein the composite product has a density less than 1 g/cm³ and an internal bond strength of at least 0.35 MPa.

63. The binder composition, method, or composite product according to any one of paragraphs 1 to 62, wherein the composite product has an internal bond strength of at least 0.35 MPa to about 5 MPa.

64. The binder composition, method, or composite product according to any one of paragraphs 1 to 63, wherein the composite product has a density of about 0.5 g/cm³ to about 1.0 g/cm³.

65. The binder composition, method, or composite product according to any one of paragraphs 1 to 64, wherein the composite product has an internal bond strength of at least 0.35 MPa to about 5 MPa and a density of about 0.5 g/cm³ to about 1.0 g/cm³.

66. The binder composition, method, or composite product according to any one of paragraphs 1 to 65, wherein the composite product comprises a particleboard, a fiberboard, a plywood, an oriented strand board, a laminated veneer lumber, parallel strand lumber, or a laminated veneer board.

67. The binder composition, method, or composite product according to any one of paragraphs 1 to 66, wherein the unsaturated compound is free from an aromatic moiety.

68. The binder composition, method, or composite product according to any one of paragraphs 1 to 67, wherein the at least one of the unsaturated carbon-carbon bonds that is a pi-bond that is not conjugated with an aromatic moiety and is capable of free radical addition is an α,β-unsaturated carbonyl, and wherein the α,β-unsaturated carbonyl comprises crotonaldehyde, 3-methylcrotonaldehyde, methacrolein, tiglic aldehyde, methyl vinyl ketone, ethyl vinyl ketone, maleic acid, itaconic acid, fumaric acid, glutaconic acid, citraconic acid, traumatic acid, muconic acid, aconitic acid, an ester of maleic acid, an ester of itaconic acid, an ester of fumaric acid, an ester of glutaconic acid, an ester of citraconic acid, an ester of traumatic acid, an ester of muconic acid, an ester of aconitic acid, acrylamide, acryloyl chloride, methacryloyl chloride, crotonoyl chloride, fumaryl chloride, itaconyl chloride, sorbic chloride, maleic anhydride, maleimide, or any mixture thereof.

69. A binder composition, comprising: at least one polyphenolic compound; at least one unsaturated compound having one or more pi-bonds that is capable of going through a radical chain reaction mechanism and is also conjugated with an aromatic moiety, and at least one free radical precursor.

70. A method for making a composite product, comprising: combining a plurality of lignocellulose substrates, at least one polyphenolic compound, at least one unsaturated compound, and at least one free radical precursor to produce a mixture, wherein the unsaturated compound comprises one or more pi-bonds that is capable of going through a radical chain reaction mechanism and is also conjugated with an aromatic moiety; and heating the mixture to a temperature of about 60° C. to about 300° C. to produce a composite product.

71. A composite product, comprising a plurality of lignocellulose substrates and an at least partially cured binder composition, wherein the binder composition, prior to at least partial curing, comprises: at least one polyphenolic compound; at least one unsaturated compound comprising one or more pi-bonds that is capable of going through a radical chain reaction mechanism and is also conjugated with an aromatic moiety, and at least one free radical precursor.

72. The binder composition, method, or composite product according to any one of paragraphs 69 to 71, wherein the unsaturated compound comprising the one or more pi-bonds that is capable of going through a radical chain reaction mechanism and is also conjugated with an aromatic moiety comprises one or more vinyl aromatics, one or more methylstyrenes, or any mixture thereof.

73. The binder composition, method, or composite product according to any one of paragraphs 69 to 71, wherein the unsaturated compound comprising the one or more pi-bonds that is capable of going through a radical chain reaction mechanism and is also conjugated with an aromatic moiety comprises styrene, methylstyrene, vinyl toluene, vinyl naphthalene, divinylbenzene (DVB), vinylpyridine, α-methylstyrene, trans-β-methylstyrene, or any mixture thereof.

74. A method for making a composite product, comprising: combining a plurality of lignocellulose substrates and a binder to produce a resinated furnish, wherein the binder comprises a polyphenolic compound, a free radical precursor, and an unsaturated compound having two or more unsaturated carbon-carbon bonds, and wherein at least one of the unsaturated carbon-carbon bonds is a pi-bond that is not conjugated with an aromatic moiety and is capable of free radical addition; pressing the resinated furnish between at least two surfaces in a press, wherein at least one of the at least two surfaces is a porous surface; and at least partially curing the binder in the resinated furnish to produce a composite product.

75. A method for making a composite product, comprising: combining a plurality of lignocellulose substrates and a binder to produce a resinated furnish, wherein the binder comprises a polyphenolic compound, a free radical precursor, and an unsaturated compound having two or more unsaturated carbon-carbon bonds, and wherein at least one of the unsaturated carbon-carbon bonds is a pi-bond that is not conjugated with an aromatic moiety and is capable of free radical addition; heating at least two surfaces in a press to a temperature of 110° C. to about 180° C., wherein at least one of the at least two surfaces is a porous surface; heating and pressing the resinated furnish between the at least two surfaces; and at least partially curing the binder in the resinated furnish to produce a composite product, wherein a core of the composite product is heated by the at least two surfaces to a maximum internal board temperature of about 100° C. to about 165° C.

76. A method for making a composite product, comprising: combining a plurality of lignocellulose substrates and a binder to produce a resinated furnish, wherein the binder comprises a polyphenolic compound, a free radical precursor, and an unsaturated compound having two or more unsaturated carbon-carbon bonds, wherein at least one of the unsaturated carbon-carbon bonds is a pi-bond that is not conjugated with an aromatic moiety and is capable of free radical addition, and wherein the unsaturated compound comprises an unsaturated polyester prepolymer, an unsaturated polyether prepolymer, an unsaturated polyamide prepolymer, an unsaturated polyurethane prepolymer, or any mixture thereof; heating and pressing the resinated furnish between at least two surfaces in a press, wherein at least one of the at least two surfaces is a porous surface, and wherein the porous surface is a press screen, a caul screen, a caul plate, a mesh screen, a press weave, or a perforated platen; and at least partially curing the binder in the resinated furnish to produce a composite product.

77. A method for making a composite product, comprising: combining a plurality of lignocellulose substrates and a binder to produce a resinated furnish, wherein the binder comprises a polyphenolic compound, a free radical precursor, and an unsaturated compound having two or more unsaturated carbon-carbon bonds, and wherein at least one of the unsaturated carbon-carbon bonds is a pi-bond that is not conjugated with an aromatic moiety and is capable of free radical addition; heating at least two surfaces in a press to a first temperature, wherein at least one of the at least two surfaces is a porous surface, heating and pressing the resinated furnish between the at least two surfaces; and at least partially curing the binder in the resinated furnish to produce a composite product, wherein a core of the composite product is heated by the at least two surfaces to a second temperature that is less than the first temperature.

78. A method for making a composite product, comprising: combining a plurality of lignocellulose substrates and a binder to produce a resinated furnish, wherein the binder comprises a polyphenolic compound, a free radical precursor, and an unsaturated compound having two or more unsaturated carbon-carbon bonds, and wherein at least one of the unsaturated carbon-carbon bonds is a pi-bond that is not conjugated with an aromatic moiety and is capable of free radical addition; heating at least two surfaces in a press to a first temperature, wherein at least one of the at least two surfaces is a porous surface, heating and pressing the resinated furnish between the at least two surfaces; producing steam from the resinated furnish; emitting the steam through the porous surface; and at least partially curing the binder in the resinated furnish to produce a composite product, wherein a core of the composite product is heated by the at least two surfaces to a second temperature that is less than the first temperature.

79. The method according to any one of paragraphs 74-78, wherein the porous surface is a press screen, a caul screen, a mesh screen, a perforated platen, a press weave, or a caul plate.

80. The method according to any one of paragraphs 74-79, wherein each of the at least two surfaces is a porous surface.

81. The method according to any one of paragraphs 74-80, wherein the at least two surfaces comprises the porous surface and a nonporous surface.

82. The method according to any one of paragraphs 74-81, wherein the porous surface comprises a plurality of openings, and wherein each opening has a mesh size of about 200 to about 8.

83. The method according to any one of paragraphs 74-82, wherein the porous surface comprises a plurality of openings, and wherein each opening has a mesh size of about 100 to about 10.

84. The method according to any one of paragraphs 74-83, wherein the porous surface comprises a plurality of openings, and wherein the porous surface has 1 to about 20 openings per linear centimeter.

85. The method according to any one of paragraphs 74-84, wherein the porous surface comprises a plurality of openings, and wherein the porous surface has 4 to about 8 openings per linear centimeter.

86. The method according to any one of paragraphs 74-85, wherein the at least two surfaces comprises a first facial contact surface and a second facial contact surface, wherein the composite product comprises a first face opposite of a second face, and wherein the first face is formed by the first facial contact surface and the second face is formed by the second facial contact surface.

87. The method according to any one of paragraphs 74-86, wherein the at least two surfaces are heated to a temperature of 110° C. to about 180° C. when at least partially curing the binder in the resinated furnish to produce the composite product.

88. The method of claim 87, wherein the resinated furnish is heated when at least partially curing the binder in the resinated furnish to produce the composite product, and wherein a core of the composite product is heated by the at least two surfaces to a maximum internal board temperature of about 100° C. to about 165° C.

89. The method of claim 88, wherein the resinated furnish is pressed to a maximum internal board pressure when at least partially curing the binder to produce the composite product, and wherein the core of the composite product is pressurized by the at least two surfaces to a maximum internal board pressure of less than 0.6 MPa.

90. The method of claim 89, wherein the maximum internal board pressure is about 0.01 MPa to about 0.22 MPa.

91. The method of claim 89, wherein the maximum internal board pressure is about 0.05 MPa to about 0.17 MPa.

92. The method according to any one of paragraphs 74-91, wherein at least partially curing the binder in the resinated furnish produces steam, and wherein at least a portion of the steam passes through the porous surface.

93. The method according to any one of paragraphs 74-92, wherein the unsaturated compound comprises an unsaturated polyester prepolymer, an unsaturated polyether prepolymer, an unsaturated polyamide prepolymer, an unsaturated polyurethane prepolymer, or any mixture thereof.

94. The method according to any one of paragraphs 74-93, wherein the composite product has an internal bond strength of at least 0.35 MPa to about 1 MPa and a density of about 0.7 g/cm³ to about 0.9 g/cm³.

95. The method according to any one of paragraphs 74-94, wherein the plurality of lignocellulose substrates comprises wood particles, wood strands, wood chips, wood flakes, wood shavings, wood wafers, or any mixture thereof.

96. The method according to any one of paragraphs 74-95, wherein the composite product is particleboard, fiberboard, oriented strand board, oriented stand lumber, chipboard, flakeboard, or waferboard.

97. The method according to any one of paragraphs 74-96, wherein the polyphenolic compound comprises one or more lignins, one or more tannins, one or more novolac resins, one or more bisphenols, one or more modified phenol formaldehyde resins, humic acid, or any mixture thereof.

98. The method according to any one of paragraphs 74-97, wherein the polyphenolic compound is modified with one or more compounds having carbon-carbon double bonds and one or more functional groups.

99. The method according to any one of paragraphs 74-98, wherein the polyphenolic compound is present in an amount of about 1 wt % to about 99 wt %, based on the combined weight of the polyphenolic compound and the unsaturated compound.

100. The method according to any one of paragraphs 74-99, wherein the unsaturated compound comprises an unsaturated polyester prepolymer.

101. The method of paragraph 100, wherein the unsaturated polyester prepolymer comprises ethylene glycol diacrylate, ethylene glycol dimethacrylate, diethylene glycol diacrylate, diethylene glycol dimethacrylate, poly(ethylene glycol)diacrylate, poly(ethylene glycol)dimethacrylate, trimethylolpropane triacrylate, pentaerythritol tetraacrylate, pentaerythritol triacrylate, or any mixture thereof.

102. The method according to any one of paragraphs 74-101, wherein the at least one of the unsaturated carbon-carbon bonds that is a pi-bond that is not conjugated with an aromatic moiety and is capable of free radical addition is an α,β-unsaturated carbonyl.

103. The method according to any one of paragraphs 74-102, wherein the unsaturated compound is present in an amount of at least 5 wt % to about 65 wt %, based on the combined weight of the polyphenolic compound and the unsaturated compound.

104. The method according to any one of paragraphs 74-103, wherein the free radical precursor comprises a mixture of one or more oxidants and one or more catalysts.

105. The method according to any one of paragraphs 74-104, wherein the free radical precursor comprises a mixture of hydrogen peroxide and one or more iron containing catalysts.

106. The method according to any one of paragraphs 74-105, wherein the one or more free radical precursors comprises one or more catalysts, and wherein the one or more catalysts comprises one or more metals in the form of a complex bound to one or more complexing agents.

107. The method according to any one of paragraphs 74-106, wherein the free radical precursor is present in an amount of at least 10 wt % to about 300 wt %, based on the weight of the unsaturated compound.

108. The method according to any one of paragraphs 74-107, wherein the free radical precursor is present in an amount of at least 5 wt % to about 200 wt %, based on the weight of the polyphenolic compound.

109. The method according to any one of paragraphs 74-108, wherein the free radical precursor is present in an amount of at least 5 wt % to about 70 wt %, based on the combined weight of the polyphenolic compound, the unsaturated compound, and the free radical precursor.

110. The method according to any one of paragraphs 74-109, wherein the polyphenolic compound is present in an amount of at least 1 wt % to about 99 wt %, wherein the unsaturated compound is present in an amount of at least 5 wt % to about 60 wt %, and wherein the free radical precursor is present in an amount of at least 5 wt % to about 70 wt %, wherein all amounts are based on the combined weight of the polyphenolic compound, the unsaturated compound, and the free radical precursor.

111. The method according to any one of paragraphs 74-11, wherein the free radical precursor comprises a mixture of hydrogen peroxide and one or more iron containing catalysts, and wherein the iron containing catalyst comprises potassium ferricyanide, iron sulfate, an iron complex of ethylenediamine tetraacetic acid, an iron complex of (S,S)-ethylenediamine-N,N′-disuccinic acid, an iron complex of diethylenetriamine pentaacetic acid, an iron complex of ethyleneglycol bis(2-aminoethylether)-N,N,N′,N′-tetraacetic acid, an iron complex of trans-1,2-diaminocyclohexanetetraacetic acid, or any mixture thereof.

Certain embodiments and features have been described using a set of numerical upper limits and a set of numerical lower limits. It should be appreciated that ranges including the combination of any two values, e.g., the combination of any lower value with any upper value, the combination of any two lower values, and/or the combination of any two upper values are contemplated unless otherwise indicated. Certain lower limits, upper limits and ranges appear in one or more claims below. All numerical values are “about” or “approximately” the indicated value, and take into account experimental error and variations that would be expected by a person having ordinary skill in the art.

Various terms have been defined above. To the extent a term used in a claim is not defined above, it should be given the broadest definition persons in the pertinent art have given that term as reflected in at least one printed publication or issued patent. Furthermore, all patents, test procedures, and other documents cited in this application are fully incorporated by reference to the extent such disclosure is not inconsistent with this application and for all jurisdictions in which such incorporation is permitted.

While the foregoing is directed to embodiments of the present invention, other and further embodiments of the invention may be devised without departing from the basic scope thereof, and the scope thereof is determined by the claims that follow. 

What is claimed is:
 1. A method for making a composite product, comprising: combining a plurality of lignocellulose substrates and a binder to produce a resinated furnish, wherein the binder comprises a polyphenolic compound, a free radical precursor, and an unsaturated compound having two or more unsaturated carbon-carbon bonds, and wherein at least one of the unsaturated carbon-carbon bonds is a pi-bond that is not conjugated with an aromatic moiety and is capable of free radical addition; pressing the resinated furnish between at least two surfaces in a press, wherein at least one of the at least two surfaces is a porous surface; and at least partially curing the binder in the resinated furnish to produce a composite product.
 2. The method of claim 1, wherein the porous surface is a press screen, a caul screen, a mesh screen, a perforated platen, a press weave, or a caul plate.
 3. The method of claim 1, wherein each of the at least two surfaces is a porous surface.
 4. The method of claim 1, wherein the at least two surfaces comprises a first facial contact surface and a second facial contact surface, wherein the composite product comprises a first face opposite of a second face, and wherein the first face is formed by the first facial contact surface and the second face is formed by the second facial contact surface.
 5. The method of claim 1, wherein the at least two surfaces are heated to a temperature of 110° C. to about 180° C. when at least partially curing the binder in the resinated furnish to produce the composite product.
 6. The method of claim 5, wherein the resinated furnish is heated when at least partially curing the binder in the resinated furnish to produce the composite product, and wherein a core of the composite product is heated by the at least two surfaces to a maximum internal board temperature of about 100° C. to about 165° C.
 7. The method of claim 6, wherein the resinated furnish is pressed to a maximum internal board pressure when at least partially curing the binder to produce the composite product, and wherein the core of the composite product is pressurized by the at least two surfaces to a maximum internal board pressure of less than 0.6 MPa.
 8. The method of claim 7, wherein the maximum internal board pressure is about 0.01 MPa to about 0.22 MPa.
 9. The method of claim 1, wherein at least partially curing the binder in the resinated furnish produces steam, and wherein at least a portion of the steam passes through the porous surface.
 10. The method of claim 1, wherein the unsaturated compound comprises an unsaturated polyester prepolymer, an unsaturated polyether prepolymer, an unsaturated polyamide prepolymer, an unsaturated polyurethane prepolymer, or any mixture thereof.
 11. The method of claim 1, wherein the composite product has an internal bond strength of at least 0.35 MPa to about 1 MPa and a density of about 0.7 g/cm³ to about 0.9 g/cm³.
 12. The method of claim 1, wherein the plurality of lignocellulose substrates comprises wood particles, wood strands, wood chips, wood flakes, wood shavings, wood wafers, or any mixture thereof, and wherein the composite product is particleboard, fiberboard, oriented strand board, oriented stand lumber, chipboard, flakeboard, or waferboard.
 13. A method for making a composite product, comprising: combining a plurality of lignocellulose substrates and a binder to produce a resinated furnish, wherein the binder comprises a polyphenolic compound, a free radical precursor, and an unsaturated compound having two or more unsaturated carbon-carbon bonds, and wherein at least one of the unsaturated carbon-carbon bonds is a pi-bond that is not conjugated with an aromatic moiety and is capable of free radical addition; heating at least two surfaces in a press to a temperature of 110° C. to about 180° C., wherein at least one of the at least two surfaces is a porous surface; heating and pressing the resinated furnish between the at least two surfaces; and at least partially curing the binder in the resinated furnish to produce a composite product, wherein a core of the composite product is heated by the at least two surfaces to a maximum internal board temperature of about 100° C. to about 165° C.
 14. The method of claim 13, wherein the porous surface is a press screen, a caul screen, a mesh screen, a perforated platen, a press weave, or a caul plate.
 15. The method of claim 13, wherein each of the at least two surfaces is a porous surface.
 16. The method of claim 13, wherein the at least two surfaces comprises a first facial contact surface and a second facial contact surface, wherein the composite product comprises a first face opposite of a second face, and wherein the first face is formed by the first facial contact surface and the second face is formed by the second facial contact surface.
 17. The method of claim 13, wherein the resinated furnish is pressed to a maximum internal board pressure when at least partially curing the binder to produce the composite product, and wherein the core of the composite product is pressurized by the at least two surfaces to a maximum internal board pressure of less than 0.25 MPa.
 18. The method of claim 13, wherein at least partially curing the binder in the resinated furnish produces steam, and wherein at least a portion of the steam passes through the porous surface.
 19. The method of claim 13, wherein the unsaturated compound comprises an unsaturated polyester prepolymer, an unsaturated polyether prepolymer, an unsaturated polyamide prepolymer, an unsaturated polyurethane prepolymer, or any mixture thereof.
 20. A method for making a composite product, comprising: combining a plurality of lignocellulose substrates and a binder to produce a resinated furnish, wherein the binder comprises a polyphenolic compound, a free radical precursor, and an unsaturated compound having two or more unsaturated carbon-carbon bonds, wherein at least one of the unsaturated carbon-carbon bonds is a pi-bond that is not conjugated with an aromatic moiety and is capable of free radical addition, and wherein the unsaturated compound comprises an unsaturated polyester prepolymer, an unsaturated polyether prepolymer, an unsaturated polyamide prepolymer, an unsaturated polyurethane prepolymer, or any mixture thereof; heating and pressing the resinated furnish between at least two surfaces in a press, wherein at least one of the at least two surfaces is a porous surface, and wherein the porous surface is a press screen, a caul screen, a caul plate, a mesh screen, a press weave, or a perforated platen; and at least partially curing the binder in the resinated furnish to produce a composite product. 